3-chlorobenzylbromide

Names

[ CAS No. ]:
766-80-3

[ Name ]:
3-chlorobenzylbromide

[Synonym ]:
Benzene, 1-(bromomethyl)-3-chloro-
EINECS 212-171-0
1-(Bromomethyl)-3-chlorobenzene
GR C1E
MFCD00000597
3-chlorobenzylbromide
α-Bromo-m-chlorotoluene

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
237.8±0.0 °C at 760 mmHg

[ Melting Point ]:
17.5ºC

[ Molecular Formula ]:
C₇H₆BrCl

[ Molecular Weight ]:
205.480

[ Flash Point ]:
103.6±10.5 °C

[ Exact Mass ]:
203.934128

[ LogP ]:
3.51

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.584

[ Storage condition ]:
Store at R.T.

[ Water Solubility ]:
DECOMPOSES

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2903999090

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Selective inhibition of heme oxygenase-2 activity by analogs of 1-(4-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole (clemizole): Exploration of the effects of substituents at the N-1 position.

Bioorg. Med. Chem. 21(21) , 6788-95, (2013)

Several analogs based on the lead structure of 1-(4-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole (clemizole) were synthesized and evaluated as novel inhibitors of heme oxygenase (HO). Many...

Selective inactivation of monoamine oxidase B by aminoethyl 3-chlorobenzyl ether. Ding CZ and Silverman RB.

Bioorg. Med. Chem. 3(10) , 2077-2078, (1993)

Convenient and robust one-pot synthesis of symmetrical and unsymmetrical benzyl thioethers from benzyl halides using thiourea. Eccles KS, et al.

ARKIVOC ix , 216-218, (2010)

4-Azido-3-chlorobenzylbromide
3-[(4-chloro-3-methyl-phenoxy)methyl]-5-(4-fluorophenyl)-4-(4-methylph enyl)-1,2,4-triazole
3-(1-thiophen-3-ylpropyl)thiophene
3-[(4-chloro-3-methylphenoxy)methyl]-4,5-bis(4-methylphenyl)-1,2,4-triazole
3-CHLORO-4-(ISOPROPYLSULFONYL)THIOPHENE-2-CARBOXYLIC ACID
3-(4-chlorophenyl)-5-[(4-methylphenoxy)methyl]-4-(4-methylphenyl)-1,2,4-triazole
2-(Propan-2-YL)cyclopropane-1-carbaldehyde
2-Imino-5-(trifluoromethyl)piperidine hydrochloride
Tetrahydro-2-[[1-methyl-1-(phenylmethyl)heptyl]oxy]-2H-pyran
2-Aminoethyl Hexadecanoate
1-(Chloroacetyl)-4-(1-phenylethyl)piperazine hydrochloride
3-(Furan-2-ylmethyl)-4-phenyl-2-(phenylamino)thiazol-3-ium bromide
5-(Bromomethyl)-2-(4-ethoxyphenyl)-4,5-dihydro-1,3-thiazole hydrobromide
N-(2-amino-4-chlorophenyl)-N,N-dimethylamine hydrochloride
4-(Chloromethyl)-2-(4-methoxyphenyl)-1,3-thiazole hydrochloride
2-(4-(Cyclopentyloxy)-5-methoxypyridin-2-yl)acetonitrile

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