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168041

Sigma-Aldrich

Cyclohexanecarbonitrile

98%

Synonym(s):

Cyanocyclohexane, Cyclohexanecarboxylic acid nitrile, Cyclohexanenitrile, Cyclohexyl cyanide, Hexahydrobenzonitrile

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About This Item

Linear Formula:
C6H11CN
CAS Number:
766-05-2
Molecular Weight:
109.17
EC Number:
212-157-4
MDL number:
MFCD00040444
UNSPSC Code:
12352100
PubChem Substance ID:
24850230
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.4505 (lit.)

bp

75-76 °C/16 mmHg (lit.)

mp

11 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

SMILES string

N#CC1CCCCC1

InChI

1S/C7H11N/c8-6-7-4-2-1-3-5-7/h7H,1-5H2

InChI key

VBWIZSYFQSOUFQ-UHFFFAOYSA-N

Application

Cyclohexanecarbonitrile was used as model substrate in rhodium-catalyzed direct ortho-arylation reactions of phenylazoles using arylboron reagents. It was used as probe in the synthesis of an asymmetric, C-magnesiated nitrile.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °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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Fraser F Fleming et al.
The Journal of organic chemistry, 71(4), 1430-1435 (2006-02-14)
Sequential carbonyl addition-conjugate addition of Grignard reagents to 3-oxocyclohex-1-ene-1-carbonitrile generates C-magnesiated nitriles whose alkylation stereoselectivities intimately depend on the nature of the electrophile. The alkylation of these C-magnesiated nitriles with alkyl halides, sulfonates, and unstrained ketones occurs with the retention
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Rhodium-catalyzed regioselective arylation of phenylazoles and related compounds with arylboron reagents via C-H bond cleavage.
Miyamura S, et al.
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