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Chemical compound
Benzyl iodide is an organic compound with the chemical formula C7H7I. The compound consists of a benzene ring with an attached iodidemethyl group. The
Benzyl_iodide
Chemical compound
Benzyl chloride Benzyl fluoride Benzyl iodide Xylyl bromide Merck Index (11th ed.). p. 1142. "Benzyl bromide_msds". William E. Bauta (2001). "Benzyl Bromide"
Benzyl_bromide
Aromatic organochlorine compound
chemical by the US Drug Enforcement Administration. Benzyl bromide Benzyl fluoride Benzyl iodide List of highly toxic gases NIOSH Pocket Guide to Chemical
Benzyl_chloride
Chemical group (–CH2–C6H5)
IUPAC nomenclature, the prefix benzyl refers to a C6H5CH2 substituent, for example benzyl chloride or benzyl benzoate. Benzyl is not to be confused with phenyl
Benzyl_group
Chemical compound
for the protection of alcohols as benzyl ethers with benzyl bromide. The solid crystal of tetra-n-butylammonium iodide is in the monoclinic crystal system
Tetra-n-butylammonium_iodide
Chemical substance
Hydrogen iodide (HI) is a diatomic molecule and hydrogen halide. Aqueous solutions of HI are known as hydroiodic acid or hydriodic acid, a strong acid
Hydrogen_iodide
Chemical compound
Benzyl fluoride is an organic compound consisting of a benzene ring substituted with a fluoromethyl group. Benzyl chloride Benzyl bromide Benzyl iodide
Benzyl_fluoride
Chemical compound
trimethylselenonium iodide used benzyl diselenide and methyl iodide. The reaction produced white crystals identified as trimethylselenonium iodide, with benzyl iodide and
Trimethylselenonium_iodide
Index of chemical compounds with the same molecular formula
The molecular formula C7H7I (molar mass: 218.03 g/mol) may refer to: Benzyl iodide Iodotoluene This set index page lists chemical structure articles associated
C7H7I
Chemical compound
Enisamium iodide is a derivative of isonicotinic acid. Based on its systematic chemical name of N-benzyl-1-methylpyridin-1-ium-4-carboxamide iodide, the shortened
Enisamium_iodide
4'-Diaminodiphenylmethane UN 2652 ? (UN No. no longer in use) UN 2653 6.1 Benzyl iodide UN 2654 ? (UN No. no longer in use) UN 2655 6.1 Potassium fluorosilicate
List of UN numbers 2601 to 2700
List_of_UN_numbers_2601_to_2700
Group of chemical compounds
in the location of the iodine, but have the same chemical formula. Benzyl iodide is an isomer, which has an iodine substituted for one of the hydrogens
Iodotoluene
Chemical compound
colorless solid. The compound is the product from the coupling of a pair of benzyl radicals. Bibenzyl forms the central core of some natural products like
Bibenzyl
French chemist (1863–1929)
by which it altered. Their work led to the use of acrolein and later benzyl iodide in weapons. Their research also had great impact and long-lasting significance
Charles_Moureu
Chemistry
chloride or an alkyl bromide to an alkyl iodide by treatment with a solution of sodium iodide in acetone. Sodium iodide is soluble in acetone while sodium chloride
Finkelstein_reaction
Benzimidazole, 4,5-dichloro-2-(trifluoromethyl)- Benzotrichloride Benzyl chloride Benzyl cyanide Bicyclo(2.2.1)heptane-2-carbonitrile Bis(chloromethyl) ketone
EPA list of extremely hazardous substances
EPA_list_of_extremely_hazardous_substances
Ion
fragment is often found for aromatic compounds containing a benzyl unit. Upon ionization, the benzyl fragment forms a cation (PhCH+ 2), which rearranges to
Tropylium_cation
Chemical group made of an –S(=O)2 group bound to a halogen
sulfonyl halides decreases in the order fluorides > chlorides > bromides > iodides, all four types being well known. The sulfonyl chlorides and fluorides
Sulfonyl_halide
New alkyl group
Sommelet and Charles R. Hauser) is a rearrangement reaction of certain benzyl quaternary ammonium salts. The reagent is sodium amide or another alkali
Sommelet–Hauser_rearrangement
Surfactant and antiseptic agent
consecutive debenzylation, dealkylation, and demethylation steps producing benzyl chloride, an alkyl dimethyl amine, dimethylamine, a long chain alkane, and
Benzalkonium_chloride
Chemical group (–CH3) derived from methane
that reacts by the SN2 pathway: CH3OH + H+ → [CH3OH2]+ Similarly, methyl iodide and methyl triflate are viewed as the equivalent of the methyl cation because
Methyl_group
Chemical compound
groups such as the benzyloxycarbonyl, 9-fluorenylmethoxycarbonyl, O- and S-benzyl and t-butylthio groups. The synthesis of 6-acetyl-1,2,3,4-tetrahydropyridine
Di-tert-butyl_dicarbonate
Chemical compound
+ O2 In common with tetraethylammonium chloride and tetraethylammonium iodide, TEAB has been used as a source of tetraethylammonium ions for numerous
Tetraethylammonium_bromide
Reaction of a glycosyl donor and acceptor
with good selectivity. The use of tetraalkylammonium iodide salts such as tetrabutylammonium iodide (TBAI) allows for in-situ anomerization of the α-glycosyl
Chemical_glycosylation
Chemical group (–C(=O)C6H5
should not be confused with benzyl, which has the formula −CH2−C6H5. The benzoyl group is given the symbol "Bz" whereas benzyl is commonly abbreviated "Bn"
Benzoyl_group
Chemical compound
from dithiane to benzyl glycidyl ether. Palladium(0)-mediated crosscoupling of vinyl iodide with the organozinc derivative of alkyl iodide afford product
Discodermolide
American chemist
the work of Hauser and Sommelet involving the rearrangement of certain benzyl quaternary ammonium salts. The reagent is sodium amide or another alkali
Charles_R._Hauser
anchoring points for fusion with the A ring. Alcohol 12 was protected by a benzyl group. The acetonide protecting group was removed from the ketone. Ketone
Danishefsky Taxol total synthesis
Danishefsky_Taxol_total_synthesis
Method for preparing ethers
catalytic quantity of a soluble iodide salt (which undergoes halide exchange with the chloride to yield a much more reactive iodide, a variant of the Finkelstein
Williamson_ether_synthesis
Medical condition of the middle ear
Nasal medications containing dilute hydrochloric acid, chlorobutanol, and benzyl alcohol have been reported to be effective in some patients, with few side
Patulous_Eustachian_tube
Cyclic chemical group (–C6H5)
Hameka, Hendrik F. (1987). "Computation of the structures of the phenyl and benzyl radicals with the UHF method". The Journal of Organic Chemistry. 52 (22):
Phenyl_group
Group of atoms introduced into a compound to prevent subsequent reactions
groups — Removed by samarium iodide, thiophenol or other soft thiol nucleophiles, or tributyltin hydride Benzylamines: Benzyl (Bn) group – Removed by hydrogenolysis
Protecting_group
Chemical species that donates an electron pair
3-epoxypropanol, 0.87 for benzyl chloride, and 1.43 for benzoyl chloride. The equation predicts that, in a nucleophilic displacement on benzyl chloride, the azide
Nucleophile
Coupling reaction
The aryl electrophile can be a halide (Br, Cl) or a triflate as well as benzyl or vinyl halides. The alkene must contain at least one sp2-C-H bond. Electron-withdrawing
Heck_reaction
Study of compounds with carbon to zinc bonds
R − X → 20 − 60 ∘ C THF R − Zn − I { R : Allyl, Aryl, Alkyl, Benzyl X : Bromide, Iodide {\displaystyle {\ce {{ZnCl2}+2K->[{\ce {THF}}][{\ce {-2KCl}}]}}\overbrace
Organozinc_chemistry
Polyatomic ion of the form >C=N< and charge +1
A.; Larsen, S. D. (1990). "Iminium Ion-Based Diels–Alder Reactions: N-Benzyl-2-Azanorborene" (PDF). Organic Syntheses. 68: 206. doi:10.15227/orgsyn.068
Iminium
isobutyric acid (C4), glycolic acid (C2), methyl bromide (C1), methyl iodide (C1), 2,3-dibromopropene (C3), acetic acid (C2) and homoallyl bromide (C4)
Mukaiyama Taxol total synthesis
Mukaiyama_Taxol_total_synthesis
Group of chemical compounds derived from alkanes containing one or more halogens
volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting
Haloalkane
described the reaction of phenyllithium and manganese(II) iodide to form phenylmanganese iodide (PhMnI) and diphenylmanganese (Ph2Mn). Following this precedent
Organomanganese_chemistry
Chemical compounds with the structure R–O–O–R'
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Peroxide
Type of organic chemical reaction
of base The reaction rate is influenced by the reactivity of halogens, iodide and bromide being favored. Fluoride is not a good leaving group, so eliminations
Elimination_reaction
Chemical compound with the group –N+≡C–
easily deprotonate at the α position. For example, benzyl isocyanide has a pKa in DMSO of 27.4 and benzyl cyanide has a pKa of 21.9, but toluene has a pKa
Isocyanide
Chemical reaction
alkyl electrophiles. Illustrative is the synthesis of benzyl cyanide by the reaction of benzyl chloride and sodium cyanide. In some cases cuprous cyanide
Cyanation
Functional group (C=O)
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Carbonyl_group
Chemical group (–CH2–CH3)
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Ethyl_group
Compound derived from an acid
reacts with sodium benzyloxide (generated from sodium and benzyl alcohol) to generate benzyl benzoate. The method is used in the production of ethyl acetate
Ester
Chemical compound
birth defects when combined with alkyl (60% C14, 25% C12, 15% C16) dimethyl benzyl ammonium chloride (ADBAC), when being fed at least 60 milligrams of disinfectant
Didecyldimethylammonium chloride
Didecyldimethylammonium_chloride
Organic compounds of the form >C=N–OH
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Oxime
Anticonvulsant and analgesic medication
name of lacosamide is (R)-2-acetamido-N-benzyl-3-methoxypropionamide and the systemic name is N2-Acetyl-N-benzyl-O-methyl-D-serinamide. Lacosamide is a
Lacosamide
Any organic compound having a sulfanyl group (–SH)
Thiols are prepared by reductive dealkylation of sulfides, especially benzyl derivatives and thioacetals. Thiophenols are produced by S-arylation or
Thiol
Organic molecule with two different functional groups
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Bifunctionality
Chemical compound
reusable. As a model reaction, the reaction of benzyl azide with 4-toluenesulfonic acid cyanide forming 1-benzyl-5-(4-toluenesulfonyl)tetrazole was investigated
Sulfolene
Organic molecule containing a neutral carbon with two unbound valence electrons
limits reaction rate. In Simmons-Smith cyclopropanation, the iodomethylzinc iodide typically complexes to any allylic hydroxy groups such that addition is
Carbene
Chemical group (R–C=O)
alkenyl groups derived from alkenes (propenyl, butenyl), or aryl groups (benzyl). Acyl compounds react with nucleophiles via an addition mechanism: the
Acyl_group
Chemical compound
chloride Names Preferred IUPAC name N-Benzyl-N,N-bis(2-hydroxyethyl)dodecan-1-aminium chloride Other names benzyl-dodecyl-bis(2-hydroxyethyl)ammonium chloride
Benzoxonium_chloride
Organic compounds of the form >C=O
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Ketone
Chemical process which generates cyclopropane rings
In the Simmons–Smith reaction the reactive carbenoid is iodomethylzinc iodide, which is typically formed by a reaction between diiodomethane and a zinc-copper
Cyclopropanation
to the amphetamine compound as Benzedrine, a term derived from the name benzyl-methyl carbinamine. In 1934, Smith, Kline & French made the first amphetamine
History and culture of substituted amphetamines
History_and_culture_of_substituted_amphetamines
Organic compound with a –C≡N functional group
nitrile synthesis is the reaction of methyl iodide with sodium cyanide to yield acetonitrile and sodium iodide: C H 3 I + N a C N ⟶ C H 3 C N + N a I {\displaystyle
Nitrile
Chemical group (–C3H7) derived from propane
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Propyl_group
Chemical compound containing carbon and at least one halogen
called organic iodides, are similar in structure to organochlorine and organobromine compounds, but the C-I bond is weaker. Many organic iodides are known
Halocarbon
competing formation of alkyisothiocyanates. "SN1-type" substrates (e.g., benzyl halides) tend to give the isothiocyanate derivatives. Some organic thiocyanates
Organic_thiocyanates
Paper on taxol synthesis
giving triol 5.5. This alcohol was monoacetylated, to give acetate 5.6. The benzyl group was removed and replaced with a triethylsilyl group. Diol 5.7 was
Nicolaou Taxol total synthesis
Nicolaou_Taxol_total_synthesis
Cleavage of C=C, C≡C, or N=N bonds with ozone
directed through a potassium iodide solution. When the solution has stopped absorbing ozone, the excess ozone oxidizes the iodide to iodine, which can easily
Ozonolysis
Chemical reaction
strongly-activated alkynes, or methyl iodide and a hindered base. Methyl iodide is also useful for hydrolysis: the alkylated hydrazonium iodide easily hydrolyzes to a
Enders SAMP/RAMP hydrazone-alkylation reaction
Enders_SAMP/RAMP_hydrazone-alkylation_reaction
Functional group with the chemical structure R–S–S–R′
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Disulfide
concentration for sodium chloride and calcium chloride, but decreases for potassium iodide and cesium chloride (the latter up to 30% mass percentage, after which viscosity
List_of_viscosities
Organosulfur compounds containing –S(=O)2–N< functional group
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Sulfonamide
Class of organic compounds
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Acetal
isobutyl, benzyl) are very reactive vinyl monomers. Studied systems are based on I2/HI and on zinc halides zinc chloride, zinc bromide and zinc iodide. In Living
Living cationic polymerization
Living_cationic_polymerization
Organic compounds of the form RC≡CC(=O)R′
cleavage of an aldehyde, followed by reaction with a hypervalent alkynyl iodide, using a gold catalyst. An alternative but longer synthetic method involves
Ynone
Organic compounds with a diazenyl group (–N=N–)
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Azo_compound
Chemical group, –C(=O)CH3
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Acetyl_group
Chemical group (–CH=CH2)
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Vinyl_group
Benzoyl chloride UN 1737 6.1 Benzyl bromide UN 1738 6.1 Benzyl chloride or Benzyl chloride unstabilized UN 1739 8 Benzyl chloroformate UN 1740 8 Hydrogen
List of UN numbers 1701 to 1800
List_of_UN_numbers_1701_to_1800
Chemical compound
Neopentyl alcohol can be converted to neopentyl iodide by treatment with triphenylphosphite/methyl iodide: (CH3)3CCH2OH + [CH3(C6H5O)3P]+I− → (CH3)3CCH2I
Neopentyl_alcohol
Group of atoms giving a molecule characteristic properties
Example functional groups of benzyl acetate: Ester group Acetyl group Benzyloxy group
Functional_group
Benzo[ghi]perylene Benzo[e]pyrene p-Benzoquinone dioxime Benzoyl peroxide Benzyl acetate Bis(1-aziridinyl)morpholinophosphine sulfide Bis(2-chloroethyl)ether
IARC_group_3
Organic compound or functional group containing a C=N bond
For example: Ieva R. Politzer and A. I. Meyers (1988). "Aldehydes from 2-Benzyl-4,4,6-trimethyl-5,6-dihydro-1,3(4H)-oxazine: 1-Phenylcyclopentanecarboxaldehyde"
Imine
Functional group
S-(2-hydroxylethyl) phenylmethanethiosulfinate, S-benzyl 2-hydroxyethane)thiosulfinate and S-benzyl phenylmethanethiosulfinate (petivericin; Ph−CH2−S(O)−S−CH2−Ph
Thiosulfinate
(INN) benzydamine (INN) Benzyl Benzoate benzylpenicillin (INN) benzylsulfamide (INN) Bepadin bepafant (INN) beperidium iodide (INN) beperminogene perplasmid
List_of_drugs:_Be-Bg
Chemical compound
GBR-13069 GBR-13098 GBR-13119 JJC8-088 MeOPP MBZP oMPP Vanoxerine Piperidines 1-Benzyl-4-(2-(diphenylmethoxy)ethyl)piperidine 2-Benzylpiperidine 2-Methyl-3-phenylpiperidine
Cytisine
Chemical group (R–S–Cl)
disulfide. Indeed, sulfenyl iodides are believed to be the active iodinating agents in iodotyrosine biosynthesis. Sulfenyl iodides that are heavily sterically
Sulfenyl_chloride
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
method, starting from epichlorohydrin. Suitable leaving groups (X) include iodide, bromide, or sulfonates. This method usually does not work well for aryl
Ether
Organosulfur compounds of the form R–SC(=O)–R′
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Thioester
Chemical reaction which transfers an alkyl group between molecules
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Transalkylation
Organic compound with an –S– group
readily alkylate to stable sulfonium salts, such as trimethylsulfonium iodide: S(CH3)2 + CH3I → [S(CH3)3]+I− Sulfides also oxidize easily to sulfoxides
Organic_sulfide
Organic compounds with a carbon-carbon-oxygen ring
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Epoxide
of acetone to ice. [citation needed] Liquid N2 Cycloheptane −12 Dry ice Benzyl alcohol −15 [citation needed] Dry ice Ethylene glycol −15 Ice Sodium chloride
List_of_cooling_baths
Chemical group (R–O)
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Alkoxy_group
Chemical reaction
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Hydrodealkylation
Class of chemical compounds
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Imide
Chemical synthesis
one asymmetric center in the process). Subsequent treatment with hydrogen iodide and red phosphorus removed the tosyl group and hydrolysed both remaining
Strychnine_total_synthesis
Drug-containing solution for intentionally ending life
clearly distinguish the solution, as well as propylene glycol, ethyl alcohol, benzyl alcohol, water, and sodium hydroxide and hydrochloric acid as needed to
Euthanasia_solution
Organic compounds of the form R–O–O–R′
Here peroxides, hydroperoxides or peracids oxidize the added potassium iodide into iodine, which reacts with starch producing a deep-blue color. Commercial
Organic_peroxides
Class of chemical compounds
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Sulfite_ester
Primary alcohol compound (CH3CH2CH2OH)
to alkyl halides; for example red phosphorus and iodine produce n-propyl iodide in 80% yield, while PCl3 with catalytic ZnCl2 gives n-propyl chloride. Reaction
1-Propanol
Any organic compound containing a C=C=C group
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Allene
Class of organic compounds
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Hydrazone
Organic compounds with the structure R–S(=O)2–OH
Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen (only C, H and O) R-O-R
Sulfonic_acid
travel, tourism, insurance
BENZYL IODIDE
BENZYL IODIDE
Boy/Male
American, Australian, British, English, Greek
A Place in Cornwall; British Town
Male
Cornish
, noble youth, or page.
Male
English
Pet form of English Benjamin, BENJY means "son of the right hand."
Boy/Male
English American
A place-name in Cornwall.
Female
English
 English gem name BERYL means "beryl," from Greek beryllos, a word applied to all green gemstones.Â
Girl/Female
English
Royal valley, referring to Kent in England.
Boy/Male
British, English
Meadow with Coarse Grass
Boy/Male
Hebrew
God builds.
Boy/Male
English American
British town.
Male
Swiss
, blessed.
Boy/Male
Polish
blessed'.
Boy/Male
Hindu
Abbreviation of benjamin and benedict
Girl/Female
American, British, English
Royal Valley; Royal Valley Referring to Kent in England
Boy/Male
Danish, German, Slavic, Swedish
Great Glory; Glorious Garland
Surname or Lastname
South German
South German : metonymic occupational name for a maker or seller of ribbons and cords, from a diminutive of Middle High German band ‘band’, ‘cord’.English : variant spelling of Bendell.
Male
German
Medieval contracted form of German Wenzeslaus, WENZEL means "more glory."
Boy/Male
African, American, Australian, British, Chinese, Christian, English, Jamaican
From Denzell; A Place-name in Cornwall; Fort; Fertile Land
Girl/Female
English American Greek
Derived from the precious stone Beryl, a gemstone of varying colors; often yellow-green. Famous...
Male
Swiss
, blessed.
Boy/Male
British, English
A Place-name in Cornwall
BENZYL IODIDE
BENZYL IODIDE
BENZYL IODIDE
BENZYL IODIDE
BENZYL IODIDE
BENZYL IODIDE
BENZYL IODIDE
n.
Striped gingham, originally brought from Bengal; Bengal stripes.
n.
The hypothetical radical, C5H11, of pentane and certain of its derivatives. Same as Amyl.
n.
A transparent, pale green variety of beryl, used as a gem. See Beryl.
n.
A phenol alcohol obtained, by the decomposition of salicin, as a white crystalline substance; -- called also hydroxy-benzyl alcohol.
n.
A compound radical, C6H5.CH2, related to toluene and benzoic acid; -- commonly used adjectively.
n.
A Bengal light.
n.
A compound radical, C6H5.CO; the base of benzoic acid, of the oil of bitter almonds, and of an extensive series of compounds.
n.
A transparent crystalline substance, C6H5.CO.NH2, obtained by the action of ammonia upon chloride of benzoyl, as also by several other reactions with benzoyl compounds.
n.
An impure benzene, used in the arts as a solvent, and for various other purposes. See Benzene.
n.
Same as Benzole.
n. sing. & pl
A native or natives of Bengal.
n .
A substance, analogous to benzil, obtained from oil of caraway.
a.
A bounding in bents, or the stalks of coarse, stiff, withered grass; as, benty fields.
n.
The language spoken in Bengal.
a.
Of or pertaining to Bengal.
n.
A compound radical, C6H5.CH, of the aromatic series, related to benzyl and benzoyl; -- used adjectively or in combination.
n.
A province in India, giving its name to various stuffs, animals, etc.
n.
A yellowish crystalline substance, C6H5.CO.CO.C6H5, formed from benzoin by the action of oxidizing agents, and consisting of a doubled benzoyl radical.
n.
A thin stuff, made of silk and hair, originally brought from Bengal.
n.
Alt. of Benzol
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