ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatic aldehydes 2-Bromobenzaldehyde

2-Bromobenzaldehyde

2-Bromobenzaldehyde Basic information
Product Name:2-Bromobenzaldehyde
Synonyms:2-BROMOBENZALDEHYDE;LABOTEST-BB LT00942758;Benzaldehyde, o-bromo-;AKOS BBS-00003178;o-Bromobenzaldehyde 2-Bromobenzaldehyde;2-Bromobenzylaldehyde;2-Bromobenzaldehyde98%;Benzaldehyde, 2-bromo-
CAS:6630-33-7
MF:C7H5BrO
MW:185.02
EINECS:229-622-2
Product Categories:Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Adehydes, Acetals & Ketones;Bromine Compounds;Aldehydes;C7;Carbonyl Compounds;Aromatic Compounds
Mol File:6630-33-7.mol
2-Bromobenzaldehyde Structure
2-Bromobenzaldehyde Chemical Properties
Melting point 16-19 °C(lit.)
Boiling point 230 °C(lit.)
density 1.585 g/mL at 25 °C(lit.)
refractive index n20/D 1.595(lit.)
Fp 203 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Liquid After Melting
Specific Gravity1.585
color Clear yellow
Water Solubility Soluble in alcohol and benzene. Insoluble in water.
FreezingPoint 14.0 to 22.0 ℃
Sensitive Air Sensitive
BRN 636132
CAS DataBase Reference6630-33-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzaldehyde, 2-bromo-(6630-33-7)
EPA Substance Registry SystemBenzaldehyde, 2-bromo- (6630-33-7)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
F 10
Hazard Note Irritant
TSCA Yes
HazardClass 6.1(b)
PackingGroup III
HS Code 29130000
MSDS Information
ProviderLanguage
o-Bromobenzaldehyde English
SigmaAldrich English
ACROS English
ALFA English
2-Bromobenzaldehyde Usage And Synthesis
Chemical Propertiesclear yellow liquid after melting
Uses2-Bromobenzaldehyde is used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
Uses2-Bromobenzaldehyde is used in L-threonine aldolase-catalyzed enantio/diastereoselective aldol reactions.
2-Bromobenzaldehyde Preparation Products And Raw materials
Preparation Products8-Bromoisoquinoline-->8-bromo-1,2,3,4-tetrahydroisoquinoline-->Methyl 2-bromobenzoate-->2-BROMOBENZYLAMINE-->2,3-dimethyl-1H-indene-->2-Diphenylphosphinobenzaldehyde-->2,3-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER-->6H-dibenzo-(b,d)-pyran-6-one-->2-(4-Pyridyl)benzaldehyde-->2-(2-Bromophenyl)-2-propanol-->4-Bromo-2-methyl-1-indanone-->8-BROMO-2H-ISOQUINOLIN-1-ONE-->2-(METHYLTHIO) BENZALDEHYDE-->1-Ethynyl-2-phenylbenzene-->BENZO(C)ACRIDINE
4(7)-BROMO-7(4)-METHYL-1-INDANONE 2-BROMOBENZALDEHYDE OXIME 3,5-Dimethoxy-4-bromobenzaldehyde 2-(ALLYLOXY)-5-BROMOBENZALDEHYDE N-ETHYLTHIOSEMICARBAZONE 3,4,5,6-TETRABROMOPHTHALIMIDE 2-BROMOBENZALDEHYDE N-(3-METHYLPHENYL)THIOSEMICARBAZONE 2-BROMOBENZALDEHYDE [3-(4-ETHOXYPHENYL)-5-SULFANYL-4H-1,2,4-TRIAZOL-4-YL]HYDRAZONE Sulfobromophthalein sodium METHYL 6-BROMO-3,4-DIMETHOXYBENZOATE Tetrabromo-2-sulfobenzoic acid cyclic anhydride LABOTEST-BB LT00012623 3-AMINO-2,4,6-TRIBROMOBENZOIC ACID 1-AMINO-4-BROMO-2-METHYLANTHRAQUINONE 3,5-BIS-(ALLYLOXY)-4-BROMOBENZALDEHYDE 2-AMINO-1-BROMO-3-CHLOROANTHRAQUINONE 2-BROMOBENZALDEHYDE DIMETHYL ACETAL 2-BROMO-6-HYDROXY-5-METHOXY-3-NITRO-BENZALDEHYDE 2,3-DIBROMO-4,5-DIHYDROXYBENZALDEHYDE
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