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7153-15-3

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7153-15-3 Usage

General Description

2-(cyclohex-1-en-1-yl)butanenitrile is a chemical compound with the molecular formula C11H15N. It is a nitrile compound that consists of a butane chain with a nitrile group (C≡N) attached to the fourth carbon, and a cyclohexene ring attached to the second carbon. 2-(cyclohex-1-en-1-yl)butanenitrile can be used in organic synthesis and chemical research as a starting material for the synthesis of other compounds. Its properties and potential uses in various industries would depend on its reactivity, stability, and toxicity, which would need to be further studied and evaluated.

Check Digit Verification of cas no

The CAS Registry Mumber 7153-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7153-15:
(6*7)+(5*1)+(4*5)+(3*3)+(2*1)+(1*5)=83
83 % 10 = 3
So 7153-15-3 is a valid CAS Registry Number.

7153-15-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohexen-1-yl)butanenitrile

1.2 Other means of identification

Product number -
Other names 2-(1'-Cyclohexenyl)-2-ethyl-acetonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7153-15-3 SDS

7153-15-3Relevant articles and documents

2,6-Piperidinediones, I: Synthesis of the Racemates and Enantiomers of 3,3-Disubstituted 2,6-Piperidinediones

Knabe, Joachim,Reischig, Dirk

, p. 353 - 362 (2007/10/02)

The synthesis of the racemates and the enantiomers of the 3,3-disubstituted 2,6-piperidinediones 3a-3g is performed in three ways, depending on the C-3 substituents.The 3-cyclohexylpiperidinedione 3h is obtained as racemic and optically active compound by

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