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Chemical compound
Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. The other two
Mesitylene
Chemical compound
(Mesitylene)molybdenum tricarbonyl is an organomolybdenum compound derived from the aromatic compound mesitylene (1,3,5-trimethylbenzene) and molybdenum
(Mesitylene)molybdenum tricarbonyl
(Mesitylene)molybdenum_tricarbonyl
Chemical reaction
example of the Zn(CN)2 method is the synthesis of mesitaldehyde from mesitylene. The Gattermann–Koch reaction, named after the German chemists Ludwig
Gattermann_reaction
Boiling points of liquid mixtures
(90th ed.). US US2530325, Carl S Carlson, "Azeotropic distillation of mesitylene from isophorone", published 14 November 1950, issued 14 November 1950
Azeotrope_tables
Chemical compound
organic compound with the formula (CH3)3C6H2Br. It is a derivative of mesitylene (1,3,5-trimethylbenzene) with one ring H replaced by Br. The compound
Mesityl_bromide
Group of isomeric chemical compounds
They also belong to the group of C3-benzenes. The best-known isomer is mesitylene. "Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume
Trimethylbenzene
Compound containing rings with delocalized pi electrons
compounds Benzene Toluene Ethylbenzene Cumene p-Xylene m-Xylene o-Xylene Mesitylene Durene Biphenyl Phenol Aniline Benzaldehyde Benzoic acid Benzamide Acetophenone
Aromatic_compound
Chemical compound
1869 Fittig and B. Wackenroder proved that the fraction is a mixture of mesitylene with another trimethylbenzene, for which the name of pseudocumol was retained
1,2,4-Trimethylbenzene
Chemical compound
acid-base adducts with even weak Lewis bases such as benzophenone and mesitylene. It forms tetrachloroaluminate ([AlCl4]−) in the presence of chloride
Aluminium_chloride
Chemical compound
isolate the aldehyde. It can also be prepared by formylation of mesitylene by reacting Mesitylene with a formyl group source such as paraformaldehyde or DMF
Mesitaldehyde
Chemical compound
trimethylphenol. The name and structure of mesitol derives from the combination of mesitylene and phenol. Mesitol is the main product from the methylation of phenol
Mesitol
Organic compounds with the formula (CH3)2C6H4
ZE2275000 ZE2625000 Related compounds Related aromatic hydrocarbons Toluene, mesitylene, benzene, ethylbenzene Related compounds Xylenols – types of phenols Except
Xylene
River in Central Europe
washed up on its shores. Water samples taken on 28 July indicated possible mesitylene contamination, although the toxin was not present in samples taken after
Oder
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Styrene
Chemical compound
acids). Uvitic acid, 5-methylisophthalic acid, is obtained by oxidizing mesitylene or by condensing pyroracemic acid with baryta water. Brown, H.C., et al
Isophthalic_acid
Hydrocarbon compound (C6H6)
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Benzene
Topics referred to by the same term
(buffer), 2-(N-morpholino)ethanesulfonic acid Mesityl group (Mes) in Mesitylene Manufacturing execution systems, to track materials Minimum efficient
MES
Organic compounds with the empirical formula CH3C6H4CH2CH3
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Ethyltoluene
Organic compound consisting entirely of hydrogen and carbon
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Hydrocarbon
Aviation fuel
testing at its pilot plant in Indiana. Composed of approximately 85% mesitylene and 15% isopentane, the fuel is reportedly scheduled for extensive testing
Avgas
Chemical compound
in (aromatic) solvents, commonly toluene but also xylene, cumene, or mesitylene, Used in large excess, it activates precatalysts for alkene polymerization
Methylaluminoxane
Chemical compound
interest as a precursor to dyes. It is prepared by selective nitration of mesitylene, avoiding oxidation of the methyl groups, followed by reduction of the
2,4,6-Trimethylaniline
Chemical reaction
reaction. The substrates are electron rich aromatic compounds, such as mesitylene or phenols, with dichloromethyl methyl ether acting as the formyl source
Rieche_formylation
Chemical compound
Electron-rich arenes are readily monochlorinated by NCS. Aniline and mesitylene are converted to the respective chlorinated derivatives. N-Iodosuccinimide
N-Chlorosuccinimide
Electric guitar played by Brian May
cold cure") (Contains formaldehyde, 1,2,4-trimethylbenzene, naphtha, mesitylene, ac412/80ip, isobutyylated melamine-formaldehyde resin.) Brian May Interview
Red_Special
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Nonacene
tetradecane 0.126 ND acetone ND 0.0019 isopropanol ND 0.0021 dioxane 0.0041 ND mesitylene 0.997 1.472 dichloromethane 0.254 0.080 ND = not determined
Solubility_of_fullerenes
Type of saturated hydrocarbon compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Alkane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
P-Cymene
Hydrocarbon compound; precursor to styrene and polystyrene
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Ethylbenzene
Chemical compound
dimer, a more soluble analogue of (benzene)ruthenium dichloride dimer. (Mesitylene)ruthenium dichloride dimer, another more soluble derivative. Bennett,
(Benzene)ruthenium dichloride dimer
(Benzene)ruthenium_dichloride_dimer
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cyclodecyne
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Isobutylene
Polycyclic aromatic hydrocarbon composed of three fused benzene rings
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Phenanthrene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Pentamethylbenzene
Organic compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cumene
Aromatic hydrocarbon
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Toluene
Chemical compound
Friedel-Crafts reaction using metal-alkyne complexes. Example, the reaction of mesitylene with phenylacetylene: Gold(III) chloride can be used for the direct oxidation
Gold(III)_chloride
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Spiropentadiene
Organic compound ((CH3)2CO); simplest ketone
consisted of mesit and ethyl alcohol. Names derived from mesit include mesitylene and mesityl oxide which were first synthesised from acetone. In 1839,
Acetone
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Diisobutene
Fish kill in Central Europe
of an oxidizing agent, and pollution by chemicals including mercury, mesitylene, salts or other sewage, as well as the possibility of an algal bloom.
2022 Oder environmental disaster
2022_Oder_environmental_disaster
Organic compound
durene (1,2,4,5-tetramethylbenzene). Isoodurene can be prepared from mesitylene, which is converted to mesityl bromide. The latter reacts with magnesium
Isodurene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
2,2,4-Trimethylpentane
Petrochemical process to break down saturated hydrocarbons in smaller molecules
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Steam_cracking
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Pentadiene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Hexamethylbenzene
Hydrocarbon compound containing one or more C=C bonds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Alkene
Index of articles associated with the same name
American gasoline contained about 3-4% C3-benzenes. Hemellitene Pseudocumene Mesitylene 1-Ethyl-2-methylbenzene 1-Ethyl-3-methylbenzene 1-Ethyl-4-methylbenzene
C3-Benzenes
Family of organic compounds
o-xylene m-xylene p-xylene Trimethylbenzenes hemimellitene pseudocumene mesitylene Tetramethylbenzenes prehnitene isodurene durene Miscellaneous ethylbenzene
Alkylbenzene
Covalent compound that contains two double bonds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Diene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cyclobutyne
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Butadiene
Chemical element with atomic number 31 (Ga)
[Ga(η6-C6Me6)]+ is that of a half-sandwich. Less bulky ligands such as mesitylene allow two ligands to be attached to the central gallium atom in a bent
Gallium
Group of chemical compounds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Tetramethylbenzene
Chemistry of compounds with Mo-C bonds
carbenes. Mo(CO)6 reacts with arenes to give piano-stool complexes such as (mesitylene)molybdenum tricarbonyl. Cycloheptatrienemolybdenum tricarbonyl, which
Organomolybdenum_chemistry
Saturated alicyclic hydrocarbon
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cycloalkane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Prismane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Methylcyclopropane
Hydrocarbon compound containing one or more C≡C bonds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Alkyne
German chemist (1835–1910)
1910) was a German chemist. He discovered the pinacol coupling reaction, mesitylene, diacetyl and biphenyl. Fittig studied the action of sodium on ketones
Wilhelm_Rudolph_Fittig
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Anthracene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Pyrene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
4-Vinyltoluene
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cymene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Naphthalene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Azulene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Tetracene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Spiropentane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
P-Xylene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Trans-Propenylbenzene
Any chemical compound having at least one gallium atom in its structure
[Ga(η6-C6Me6)]+ is that of a half-sandwich. Less bulky ligands such as mesitylene allow two ligands to be attached to the central gallium atom in a bent
Gallium_compounds
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
O-Xylene
Index of chemical compounds with the same molecular formula
4-Ethyltoluene Trimethylbenzenes 1,2,3-Trimethylbenzene 1,2,4-Trimethylbenzene Mesitylene (1,3,5-trimethylbenzene) Ethylidene norbornene Tetravinylmethane Vinyl
C9H12
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
2-Methylpentane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cyclohexyne
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Phenylacetylene
Organic compound, C6H4(CH=CH2)2
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Divinylbenzene
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Pentacene
Hydrocarbon composed of multiple aromatic rings
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
Molecule consisting of three identical molecules bound together
sulfuric acid, trimerization of acetone via aldol condensation affords mesitylene Dimethylsilanediol dehydrates to a trimer of Me2SiO as well as polydimethylsiloxane
Trimer_(chemistry)
Chemical reaction
excellent phenoxide nucleophiles. Other electron-rich substrates, such as mesitylene, pyrrole, or fused aromatic rings can also be expected to react. Benzene
Formylation
Chemical compound
(phenyldimethylacetic acid) With p-cymene ethylsodium adds sodium to the methyl group. Mesitylene yields 3,4-dimethylphenlsodium. With diphenylmethane, sodium substitutes
Ethylsodium
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
1,5-Hexadiene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
N-Butylbenzene
Chemical compound
Saturated solution of Fe3(CO)12 in mesitylene.
Triiron_dodecacarbonyl
Organic compound (H2C=C=CH2)
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Propadiene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
N-Propylbenzene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
2-Methylhexane
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
4-Ethyltoluene
Chemical compound
only with stronger aminating agents such as O-tosylhydroxylamine or O- mesitylene sulfonylhydroxylamine to amino compounds, which were investigated as explosives
Hydroxylamine-O-sulfonic_acid
Organic compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Tert-Butylbenzene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
1-Decyne
Synthetic plant growth regulator
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
1-Methylcyclopropene
Hydrocarbon compound with 3 or more consecutive double bonds
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Cumulene
Oxyacid of phosphorus
effective reagent for the hydroxylation of aromatic rings. The conversion of mesitylene to mesitol can be achieved at room temperature in less than four hours
Peroxymonophosphoric_acid
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
1,2,3-Trimethylbenzene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
Methylcyclopentane
Cage-like allotrope of carbon
3 × 10−11 pentane 0.004 octane 0.025 isooctane 0.026 decane 0.070 dodecane 0.091 tetradecane 0.126 dioxane 0.0041 mesitylene 0.997 dichloromethane 0.254
Buckminsterfullerene
Chemical compound
o-Xylene m-Xylene p-Xylene Other Ethylbenzene C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes
M-Xylene
MESITYLENE
MESITYLENE
MESITYLENE
MESITYLENE
Girl/Female
Hindu
Best, The Goddess who is above the five elements
Boy/Male
Hindu
Sum of the Vedas
Girl/Female
Hindu, Indian, Marathi
Wave; Humming of a Bee
Boy/Male
Spanish
Tranquil.
Boy/Male
Arabic, Punjabi
Glory; Destiny
Boy/Male
Arabic
Intelligence; Wisdom; Learning the Quran by Heart
Biblical
forgetfulness; desertionmarsh
Boy/Male
German
Powerful ruler.
Biblical
same as Paul
Girl/Female
English
From the royal meadow.
MESITYLENE
MESITYLENE
MESITYLENE
MESITYLENE
MESITYLENE
a.
Of, pertaining to, or designating, a tribasic acid, C6H3.(CO2)3, of the aromatic series, obtained, by the oxidation of mesitylene, as a white crystalline substance.
n.
A hydrocarbon of the aromatic series, metameric with mesitylene and cumene, found in coal tar, and obtained as a colorless liquid.
n.
A colorless, fragrant liquid, C6H3(CH3)3, of the benzene series of hydrocarbons, obtained by distilling acetone with sulphuric acid.
a.
Pertaining to, or designating, an acid, CH3C6H3(CO2H)2, obtained as a white crystalline substance by the partial oxidation of mesitylene; -- called also mesitic acid.
n.
A crystalline substance obtained from mesitylene.
a.
Pertaining to, derived from, or related to, xylene; specifically, designating any one of several metameric acids produced by the partial oxidation of mesitylene and pseudo-cumene.
n.
A rearrangement or concentration of the different constituents of one or more substances into a distinct and definite compound of greater complexity and molecular weight, often resulting in an increase of density, as the condensation of oxygen into ozone, or of acetone into mesitylene.