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115959

Sigma-Aldrich

Benzoyl cyanide

98%

Synonym(s):

Phenylglyoxylonitrile

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About This Item

Linear Formula:
C6H5COCN
CAS Number:
613-90-1
Molecular Weight:
131.13
Beilstein:
1072101
EC Number:
210-359-7
MDL number:
MFCD00001837
UNSPSC Code:
12352100
PubChem Substance ID:
24847253
NACRES:
NA.22

Assay

98%

form

solid

bp

206 °C (lit.)

mp

28-31 °C (lit.)

density

1.106 g/mL at 25 °C (lit.)

SMILES string

O=C(C#N)c1ccccc1

InChI

1S/C8H5NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H

InChI key

GJQBHOAJJGIPRH-UHFFFAOYSA-N

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General description

Benzoyl cyanide is used to study the mechanism of reduction of benzoyl cyanide in acetonitrile, N,N-dimethylformamide and acetonitrile. It undergoes hydrolysis by Rhodococcus sp. CCZU10-1 to form benzoylformic acid.

Application

Reagent for selective acylation of amino compounds.

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Description
Pricing

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H300

Precautionary Statements

P264 - P301 + P310

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

183.2 °F - closed cup

Flash Point(C)

84 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yi Xu et al.
Journal of virology, 92(11) (2018-03-09)
Translational readthrough of the stop codon of the capsid protein (CP) open reading frame (ORF) is used by members of the Luteoviridae to produce their minor capsid protein as a readthrough protein (RTP). The elements regulating RTP expression are not
Konstantin N Bulygin et al.
RNA (New York, N.Y.), 22(2), 278-289 (2015-12-15)
Translation termination in eukaryotes is mediated by release factors: eRF1, which is responsible for stop codon recognition and peptidyl-tRNA hydrolysis, and GTPase eRF3, which stimulates peptide release. Here, we have utilized ribose-specific probes to investigate accessibility of rRNA backbone in
Synthesis, 433-433 (1993)
Weisi Xiong et al.
Biotechnology letters, 37(8), 1703-1709 (2015-04-22)
To develop a biphasic system for use in plant tissue-mediated biotransformations to overcome the low water solubilities of substrates and inhibitory effects of products. Commonly-used organic solvents and ionic liquid were assayed using the biphasic system to reduce water-insoluble benzoyl
Norma A Macías-Ruvalcaba et al.
The Journal of organic chemistry, 72(2), 589-594 (2007-01-16)
The mechanism of reduction of benzoyl cyanide, 6, p-methoxybenzoyl cyanide, 7, and p-chlorobenzoyl cyanide, 8, has been studied in acetonitrile (6 and 7), N,N-dimethylformamide (6), and acetonitrile containing water (all three compounds). The reaction proceeds by initial reduction to form
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