2-Cyanobenzyl bromide

Names

[ Name ]:
2-Cyanobenzyl bromide

[Synonym ]:
O-CYANOBENZYL BROMIDE
α-Bromo-o-tolunitrile
Benzonitrile, 2-(bromomethyl)-
o-Tolunitrile, α-bromo-
2-Cyanobenzyl Bromide
alpha-Bromo-o-tolunitrile
1-cyano-2-bromomethyl benzene
A-BROMO-O-TOLUNITRILE
2-(Bromomethyl)benzonitrile
2-(Brommethyl)benzolcarbonitril
2-(3-FLUOROBENZYLOXY)-5-NITROBENZALDEHYDE
2-bromomethyl-benzonitrile
2-Cyanobenzylbromide
o-bromomethylbenzonitrile
NCR B1E
MFCD00001794
EINECS 231-555-8
Letrozole Impurity 5

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
264.6±15.0 °C at 760 mmHg

[ Melting Point ]:
72-74 °C(lit.)

[ Molecular Formula ]:
C₈H₆BrN

[ Molecular Weight ]:
196.044

[ Flash Point ]:
113.8±20.4 °C

[ Exact Mass ]:
194.968353

[ PSA ]:
23.79000

[ LogP ]:
2.36

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.588

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

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

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C:Corrosive

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45-S28A

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2926909090

Precursor & DownStream

Precursor

DownStream

Preparation

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.

J. Comb. Chem. 11 , 14-33, (2009)

Distributed Drug Discovery (D(3)) proposes solving large drug discovery problems by breaking them into smaller units for processing at multiple sites. A key component of the synthetic and computationa...

Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c]isoquinolin- 5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one.

Org. Lett. 7(9) , 1753-6, (2005)

[reaction: see text] The synthesis of 6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-ones from the base-promoted condensation reaction of homophthalic anhydride and 2-(bromomethyl)-benzonitrile and a conv...

4-[(2H-Tetra-zol-2-yl)meth-yl]benzonitrile.

Acta Crystallogr. Sect. E Struct. Rep. Online 64(Pt 2) , o445, (2008)

The title compound, C(9)H(7)N(5), was synthesized by reaction of 4-(bromomethyl)benzonitrile and 2H-tetrazole in the presence of KOH. The relative orientation of the planar tetra-zole ring and the met...