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Chemical compound
5-Decyne, also known as dibutylethyne, is a type of alkyne with a triple bond at its fifth carbon (the '5-' indicates the location of the triple bond
5-Decyne
Index of chemical compounds with the same name
Decynes are alkynes with one triple bond and the molecular formula C10H18. The isomers are: 1-Decyne 2-Decyne [Wikidata] 3-Decyne 4-Decyne 5-Decyne This
Decyne
Chemical compound
colorless liquid is one of three isomeric hexynes. 3-Hexyne forms with 5-decyne, 4-octyne, and 2-butyne a series of symmetric alkynes. It is a reagent
3-Hexyne
Chemical compound
the triple bond in the chain). Its formula is C8H14. 4-Octyne forms with 5-decyne, 3-hexyne, and 2-butyne a group of symmetric alkynes. One method for synthesizing
4-Octyne
Alkyne with four carbon atoms
have been recorded and analysed. 2-Butyne (dimethylethyne) forms with 5-decyne (dibutylethyne), 4-octyne (dipropylethyne) and 3-hexyne (diethylethyne)
2-Butyne
Chemical compound
1-Decyne is the organic compound with the formula C8H17C≡CH. It is a terminal alkyne. A colorless liquid, 1-decyne is used as a model substrate when evaluating
1-Decyne
Index of chemical compounds with the same molecular formula
C10H18 may refer to: Bornane Cyclodecene Decalin Decynes 1-Decyne 2-Decyne 3-Decyne 4-Decyne 5-Decyne, also known as dibutylethyne Spirodecane This set
C10H18
Chemical compound
centers. Illustrative complexes are (azulene)Mo2(CO)6 and (azulene)Fe2(CO)5. 1-Hydroxyazulene is an unstable green oil and it does not show keto–enol
Azulene
Organic compounds with the formula (CH3)2C6H4
manufacture of coke fuel. They also occur in crude oil in concentrations of about 0.5–1%, depending on the source. Small quantities occur in gasoline and aircraft
Xylene
Compound containing rings with delocalized pi electrons
the equivalent nature of the six carbon-carbon bonds all of bond order 1.5. This equivalency can also explained by resonance forms. The electrons are
Aromatic_compound
Chemical compound
plastics industry". Occupational and Environmental Medicine. 52 (5): 320–7. doi:10.1136/oem.52.5.320. PMC 1128224. PMID 7795754. Danish EPA 2011 review "Archived
Styrene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cumene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
2,2,4-Trimethylpentane
Polycyclic aromatic hydrocarbon composed of three fused benzene rings
diphenylaldehyde Phenanthrene is extracted from coal tar, of which it comprises 5% by weight. In principle it could be obtained by chemical synthesis. The Bardhan–Sengupta
Phenanthrene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cyclopropyne
Petrochemical process to break down saturated hydrocarbons in smaller molecules
to drive its steam turbines. A typical world scale ethylene plant (about 1.5 billion pounds (680 KTA) of ethylene per year) uses a 45,000 horsepower (34
Steam_cracking
Chemical compound
3-pentadiene releases only 26.5 kcal/mol, implying a very similar value of 3.6 kcal/mol for the stabilization energy. The ~3.5 kcal/mol difference in these
Butadiene
Aromatic hydrocarbon
(NIOSH). Haynes, p. 5.164 Haynes, p. 5.176 Haynes, p. 3.579 Haynes, p. 6.258 Haynes, p. 6.246 Haynes, p. 9.66 Haynes, pp. 5.39, 5.67 Haynes, p. 16.30
Toluene
Hydrocarbon compound containing one or more C≡C bonds
hydration of 1,8-nonadiyne to 2,8-nonanedione: HC ≡ C ( CH 2 ) 5 C ≡ CH + 2 H 2 O ⟶ CH 3 CO ( CH 2 ) 5 COCH 3 {\displaystyle {\ce {HC#C(CH2)5C#CH + 2H2O -> CH3CO(CH2)5COCH3}}}
Alkyne
Chemical compound
freitalite and is related to a coal deposit. Coal tar, which contains around 1.5% anthracene, remains a major industrial source of this material. Common impurities
Anthracene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
M-Cymene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
2-Methylpentane
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
P-Xylene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
1,5-Hexadiene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
4-Vinyltoluene
Chemical compound
Thieme Verlag. p. 615. doi:10.1055/sos-SD-048-00343. ISBN 978-3-13-119021-5. Retrieved 6 April 2026. Connor, Daniel S.; Wilson, Eugene R. (1 January 1967)
Methylcyclobutane
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Sec-Butylbenzene
Hydrocarbon compound containing one or more C=C bonds
propylene only C4H8: 3 isomers: 1-butene, 2-butene, and isobutylene C5H10: 5 isomers: 1-pentene, 2-pentene, 2-methyl-1-butene, 3-methyl-1-butene, 2-methyl-2-butene
Alkene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Tert-Butylbenzene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Isobutylbenzene
Organic compound (H2C=C=CH2)
methylacetylene-propadiene: H3C−C≡CH ⇌ H2C=C=CH2 for which Keq = 0.22 at 270 °C or 0.1 at 5 °C. MAPD is produced as a side product, often an undesirable one, of dehydrogenation
Propadiene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Tetracene
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Pentadiene
Hydrocarbon composed of multiple aromatic rings
Fluorene Acenaphthene Acenaphthylene Fluoranthene Helicenes [4]Helicene [5]Helicene [10]Helicene Circulenes Corannulene Coronene Kekulene Large networks
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
N-Butylbenzene
Chemical compound
Isolation of Spiropentane1". Journal of the American Chemical Society. 66 (5): 812–816. Bibcode:1944JAChS..66..812M. doi:10.1021/ja01233a047. ISSN 0002-7863
Spiropentane
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Trans-Propenylbenzene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
2-Methyloctane
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
O-Xylene
Organic compound, C6H4(CH=CH2)2
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Divinylbenzene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
N-Propylbenzene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
O-Cymene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cyclooctyne
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Octacene
Chemical compound
ISBN 978-0-85404-182-4. "M-Xylene". pubchem.ncbi.nlm.nih.gov. Retrieved 5 June 2026. NIOSH Pocket Guide to Chemical Hazards. "#0669". National Institute
M-Xylene
Hydrocarbon compound (CH3–CH=CH–CH=CH2)
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Piperylene
Chemical compound
1021/ja00876a047 Fort, Raymond C. Adamantane. Studies in Organic Chemistry. Vol. 5. New York, NY: Marcel Dekker. pp. 114–115. A new synthesis of twistane Jean
Twistane
Chemical compound
Book of Chemical and Physical Data. CRC Press. p. 544. ISBN 978-0-8493-0595-5. Stanley R. Sandler, Wolf Karo (2012). Sourcebook of Advanced Organic Laboratory
1,3,5-Triethylbenzene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
1,7-Octadiene
Organic compounds with the empirical formula CH3C6H4CH2CH3
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Ethyltoluene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Mesitylene
Covalent compound that contains two double bonds
stability. For example, deprotonation at position 3 of a 1,4-diene or position 5 of a 1,3-diene give a pentadienyl anion. An even greater effect is seen if
Diene
Synthetic plant growth regulator
interacting with the ethylene receptor in plants". Plant Biol. 5 (5): 473–80. Bibcode:2003PlBio...5..473S. doi:10.1055/s-2003-44782. S2CID 260252729. 1-Methylcyclopropene
1-Methylcyclopropene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
2-Methylhexane
Chemical compound
followed by treatment with lead tetraacetate affords the unsaturated basketene (5), which is then hydrogenated to basketane (6). An alternative synthetic route
Basketane
Hydrocarbon compound with 3 or more consecutive double bonds
was (Ph2C2Fe2(CO)8, derived from the reaction of diphenylketene and Fe(CO)5. Structurally, this molecule resembles Fe2(CO)9, wherein one μ-CO ligand is
Cumulene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Housane
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
with a high application potential due to a hole mobility in OFETs of up to 5.5 cm2/(V·s), which exceeds that of amorphous silicon. Pentacene, as well as
Pentacene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Hexacene
Class of chemical compounds
organic field-effect transistors, reaching charge carrier mobilities as high as 5 cm2/V s. The first unsubstituted members are listed in the following table:
Acene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
1,2,3-Trimethylbenzene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Durene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
2-Phenylhexane
Hydrocarbon ring molecule containing a C≡C bond
guanacastapenes O and N. It allowed for the expedient construction of the 5-7-6 ring system and provided useful synthetic handles for subsequent functionalization
Cycloalkyne
Family of organic compounds
models of complex processes. Cham, Switzerland: Springer. ISBN 978-3-030-99746-5. OCLC 1333919856. Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges,
Alkylbenzene
Chemical compound
Characterized Acenes". Angewandte Chemie International Edition. 49 (24): 4012–5. doi:10.1002/anie.200906002. PMID 20468014. Clar, E. (1942). "Heptacen ein
Heptacene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cyclopentyne
Chemical compound
Pentamethylbenzene is an organic compound with the formula C6H(CH3)5. It is a colourless solid with a sweet odor. The compound is classified as an aromatic
Pentamethylbenzene
Index of articles associated with the same name
g/mol. C4-benzenes are found in petroleum. Petrol (gasoline) can contain 5-8% C4-benzenes. o-Cymene m-Cymene p-Cymene Prehnitene Isodurene Durene 1-Ethyl-2
C4-Benzenes
Chemical compound
al. "Detection of Cyclopropenylidene on Titan with ALMA" J. Astron., 160-5 (2020) Maguire, W. C.; Hanel, R. A.; Jennings, D. E.; Kunde, V. G.; Samuelson
Cyclopropenylidene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cyclononyne
Conjugated hydrocarbon ring molecules with at least one triple bond
spectroscopic data the products formed were in fact two linear 1,3-hexadien-5-yne isomers and not macrocycles. Computational analysis of this compound suggests
Annulyne
Chemical compound
1039/9781849733069. ISBN 978-0-85404-182-4. Haynes, p. 3.472 Haynes, p. 5.162 Haynes, p. 5.176 Haynes, p. 12.96 Haynes, p. 3.579 Camerman, A.; Trotter, J. (1965)
Pyrene
Chemical compound
Properties of Kekulene". Angewandte Chemie International Edition in English. 17 (5): 372–374. doi:10.1002/anie.197803721. Jiao, Haijun; Schleyer, Paul von Ragué
Kekulene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cyclodecyne
Organic compound consisting entirely of hydrogen and carbon
OCLC 288470227. "Benzene global market volume 2015-2026". Statista. Retrieved 5 December 2021. Nunes, T.M.; Turatti, I.C.C.; Mateus, S.; Nascimento, F.S.;
Hydrocarbon
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Pentaphene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
4-Ethyltoluene
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Diisobutene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Cycloheptyne
Chemical compound
chlorocarbene generated from methyllithium and dichloromethane to spiro compound 5. Spiropentadiene was trapped in a liquid nitrogen trap after reaction with
Spiropentadiene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Nonacene
Hydrocarbon compound; precursor to styrene and polystyrene
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Ethylbenzene
Saturated alicyclic hydrocarbon
Owing to the nature polygons, rings with 3, 4, and (to a small extent) also 5 atoms can only afford narrower interior angles; the consequent deviation from
Cycloalkane
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Isobutylene
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Methylcyclopentane
Chemical compound
(97th ed.). Boca Raton, Florida: CRC Press. pp. 3–304, 3–578, 5–29, 5–67, 5–158, 5–175, 5–180, 6–77, 6–95, 6–149, 6–159, 8–38, 12–96, 16–27, 16–40. ISBN 9781498754293
Naphthalene
Chemical compound
acidic copper(II) chloride. Neutralized with a strong base, the azo compound (5) could be crystallized with 65% yield. The last step is a photolysis of the
Prismane
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Phenylacetylene
Chemical reaction
and tetrakis(triphenylphosphine)palladium(0), 5,7-hexadecadiene from 1-decyne and (Z)-1-hexenyl iodide. Negishi coupling has been applied in the synthesis
Negishi_coupling
Hydrocarbon compound (C6H6)
produces biphenyl (diphenyl) at higher temperature: 2 C 6H 6 ⇌ H 2 + C 6H 5–C 6H 5 If the raw material stream contains much non-aromatic components (paraffins
Benzene
Chemical compound
and the applications of bis(η6-arene) complexes". Coord. Chem. Rev. 254 (5–6): 402–419. doi:10.1016/j.ccr.2009.05.014. Kotz, John C. (1986). "The Electrochemistry
Hexamethylbenzene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Prehnitene
Organic compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
Isodurene
Type of saturated hydrocarbon compound
arbitrarily large and complex molecules, like hexacontane (C60H122) or 4-methyl-5-(1-methylethyl) octane, an isomer of dodecane (C12H26). The International
Alkane
Chemical compound
it is a minor additive, with its share in US gasoline rising from 0.03%–0.5% in early 1990s to 1.1%–2.6% in 2011. It may be a major component of some
1,2,4-Trimethylbenzene
Chemical compound
Chemical Physics. 157 (24): 244501. Bibcode:2022JChPh.157x4501P. doi:10.1063/5.0133511. PMID 36586992. Balahbib, Abdelaali; El Omari, Nasreddine; Hachlafi
P-Cymene
Chemical compound
trimethylphosphine. Parker, W. (31 October 2007). Alicyclic Chemistry: Volume 5. Royal Society of Chemistry. p. 248. ISBN 978-1-84755-548-9. Retrieved 29
Cyclohexyne
Chemical compound
Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne Isohexyne Isoheptyne Isooctyne Isononyne Isodecyne
1,3,5-Triheptylbenzene
5 DECYNE
5 DECYNE
Boy/Male
Muslim
One who prays 5 times and fasts, Forever, Immortal
Boy/Male
Hindu, Indian, Tamil
5 Head of Snake
Male
Japanese
(1-æ£, 2-é›…, 3-昌, 4-真, 5-政, 6-å°†) Unisex short form of Japanese names beginning with Masa-, MASA means 1) "correct, just," 2) "elegant, splendid" 3) "flourishing, prosperous" 4) "genuine, true," 5) "governing, political," 6) "military." Compare with another form of Masa.
Surname or Lastname
English
English : occupational name for a maker or seller of hoods, from Middle English hodestre, a feminine form of Hodder.German (also Höster) : habitational name for someone from either of two places called Host (see Host 5).
Girl/Female
Assamese, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
A Garland of 5 Types of Flowers
Surname or Lastname
English (Yorkshire)
English (Yorkshire) : unexplained.French : from a diminutive of Bard 5.Hungarian (Bárdy) : habitational name for someone from a place called Bárd in Somogy county or in Máramaros, (now Maramures in Romania).
Female
Japanese
(1-æµ, 2-æ…¶, 3-æ¡‚, 4-敬, 5-å•“, 6-åœ, 7-景) Japanese name KEI means 1) "blessed, lucky," 2) "happy," 3) "katsura tree," 4) "respectful," 5) "spring," 6) "square jewel," or "sunny."Â
Surname or Lastname
English
English : patronymic from Kay 5.
Male
Japanese
(1-ç´€, 2-ä¿®, 3-ç†, 4-åŽ, 5-æ²», 6-çµ±) Japanese name OSAMU means 1) "chronicler," 2) "disciplined," 3) "logical," 4) "obtainer," 5) "to reign," 6) "ruler."
Surname or Lastname
German
German : diminutive of Summer 5.English (Bedfordshire) : unexplained.
Surname or Lastname
English
English : nickname from Middle English dull + -ard ‘dull or stupid person’. Compare Doll 5.Irish : either an importation to Ireland of the English name or, possibly, a reduced and altered form of de la Hyde (see Dollarhide).
Surname or Lastname
English
English : variant spelling of Peak.Irish : variant of Peak 2.North German : metonymic occupational name for a spearmaker, from Middle Low German pēk ‘pike’. Compare Pike 4.Dutch : variant of Peck 4 and 5.
Female
Japanese
(1-æ£, 2-é›…, 3-昌, 4-真, 5-政, 6-å°†) Unisex short form of Japanese names beginning with Masa-, MASA means 1) "correct, just," 2) "elegant," 3) "flourishing, prosperous" 4) "genuine, true," 5) "governing, political," 6) "military." Compare with strictly masculine Masa.
Female
Japanese
(1-æµå, 2-æ…¶å, 3-æ¡‚å, 4-敬å, 5-å•“å, 6-åœå, 7-景å) Japanese name KEIKO means 1) "blessed, lucky child," 2) "happy child," 3) "katsura tree child," 4) "respectful child," 5) "spring child," 6) "square jewel child," or 7) "sunny child."
Male
Japanese
(1-æµ, 2-ä½³, 3-敬, 4-åœ, 5-æ…§) Japanese name KEI means 1) "blessed, lucky," 2) "excellent," 3) "respect," 4) "square jewel," or 5) "wise."
Surname or Lastname
English
English : variant spelling of Kay 4 and 5.
Male
Japanese
(1-晋, 2-信, 3-紳, 4-心, 5-慎, 6-新, 7-進, 8-真) Japanese name SHIN means 1) "advancing," 2) "belief," 3) "gentleman," 4) "heart," 5) "humble," 6) "new," 7) "progressive," and 8) "true." Compare with another form of Shin.
Surname or Lastname
South German (Düll)
South German (Düll) : nickname for a stubborn man.German (Düll) : variant of Dill 5.English : unexplained.
Surname or Lastname
English
English : variant of Wall.Swedish : ornamental name composed of the elements wall, an old spelling of vall ‘grassy bank’ + man ‘man’.German (Wallmann) : variant of Wall 4 and 5.
Male
Japanese
(1-æš, 2-æ‚Ÿ, 3-è¡, 4-知, 5-覚, 6-è«, 7-了, 8-智) Japanese name SATORU means 1) "daybreak," 2) "enlightened," 3) "fast learner," 4) "knowledgeable," 5) "perceptive," 6) "persuasive," 7) "understanding," or 8) "wise."
5 DECYNE
5 DECYNE
Boy/Male
Hindu, Indian
A Legend
Girl/Female
Indian
Grace, Kindness, Favor, Gift
Girl/Female
Arabic, Muslim
The Best Part
Boy/Male
Tamil
Sreekumar | à®·à¯à®°à¯€à®•à¯à®®à®¾à®°
Wealthy person
Boy/Male
Hindu, Indian
Well Lit Blazing Brightly
Boy/Male
Finnish, French, Hindu, Indian, Sanskrit
Bowed
Girl/Female
Indian, Telugu
Teachings
Surname or Lastname
English
English : variant of the English habitational name Bayldon.English : possibly also a variant of Balding.English : Many if not all bearers of this surname are descended from Richard Bayldon, who came from England to CT in 1645.
Girl/Female
Hindu
With a sound mind, A lady
Boy/Male
Arabic
Big
5 DECYNE
5 DECYNE
5 DECYNE
5 DECYNE
5 DECYNE
n.
A way for passage; a hall. See Passage, 5.
n.
A morality play. See Morality, 5.
n.
See Romance, 5.
n.
Same as Placard, 4 & 5.
n.
See 4th Trap, 5.
n.
The thorax of an insect. See Trunk, n., 5.
n.
See Tailing, n., 5.
n.
See Tread, n., 5.
n.
An umbilicus. See Umbilicus, 5 (b).
n. & v.
See Prize, n., 5. Also Prize, v. t.
n.
See Closure, 5.
pref.
On; along; in traversing. Compare 5.
n.
See Flyer, n., 5.
a.
Affected with the vapors. See Vapor, n., 5.
n.
See Relief, n., 5.
n.
Same as Gudgeon, 5.
v.
See Affected, 5.
n.
See Camp, n., 5.
n.
Same as Relief, n., 5.
n.
Same as Reed, n., 5.