Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

144711

Sigma-Aldrich

2-(Bromomethyl)benzonitrile

≥97%

Synonym(s):

α-Bromo-o-tolunitrile, 2-Cyanobenzyl bromide

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
$35.42
25 G
$165.00

$35.42

List price$50.60Save 30%
Web-Only Promotion

Available to ship onApril 08, 2025Details

Request a Bulk Order
All Photos(1)

Select a Size

Change View
5 G
$35.42
25 G
$165.00

About This Item

Linear Formula:
BrCH2C6H4CN
CAS Number:
22115-41-9
Molecular Weight:
196.04
Beilstein/REAXYS Number:
742605
MDL number:
MFCD00001794
UNSPSC Code:
12352100
PubChem Substance ID:
24848680
NACRES:
NA.22

$35.42

List price$50.60Save 30%
Web-Only Promotion

Available to ship onApril 08, 2025Details

Request a Bulk Order

assay

≥97%

form

solid

mp

72-74 °C (lit.)

functional group

bromo
nitrile

SMILES string

BrCc1ccccc1C#N

InChI

1S/C8H6BrN/c9-5-7-3-1-2-4-8(7)6-10/h1-4H,5H2

InChI key

QGXNHCXKWFNKCG-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2-(Bromomethyl)benzonitrile reacts with 2H-tetrazole in the presence of KOH to yield 4-[(2H-tetra-zol-2-yl)meth-yl]benzonitrile[1]. It undergoes base-promoted condensation reaction with homophthalic anhydride to yield 6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-one[2].

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBD7205V
S43607
25016MQ
19622DB
12718JO

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Prakash G Jagtap et al.
Organic letters, 7(9), 1753-1756 (2005-04-23)
[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 convenient method for the synthesis of indolo[3,2-c]isoquinolinones are described.
Zheng Xing et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 2), o445-o445 (2008-01-01)
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 methyl-benzonitrile moiety is (-)-anti-clinal. The crystal packing is dominated by van der Waals
William L Scott et al.
Journal of combinatorial chemistry, 11(1), 14-33 (2008-12-25)
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 computational stages of D(3) is the global rehearsal of prospective reagents and

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service