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2-(pyrrolidin-1-yl)cyclohex-1-en carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160361-75-1

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160361-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160361-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,3,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 160361-75:
(8*1)+(7*6)+(6*0)+(5*3)+(4*6)+(3*1)+(2*7)+(1*5)=111
111 % 10 = 1
So 160361-75-1 is a valid CAS Registry Number.

160361-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(pyrrolidin-1-yl)cyclohex-1-en carbonitrile

1.2 Other means of identification

Product number -
Other names 2-pyrrolidino-1-cyclohexene-1-carbonitrile

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:160361-75-1 SDS

160361-75-1Downstream Products

160361-75-1Relevant academic research and scientific papers

A new and facile synthesis of methyl 3-amino-4,5,6,7-tetrahydrobenzo[b] thiophene-2-carboxylate

Tenora, Luká?,Buchlovi?, Marian,Man, Stanislav,Potá?ek, Milan

supporting information; experimental part, p. 401 - 403 (2011/02/28)

A four-step synthesis of methyl 3-amino-4,5,6,7-tetrahydrobenzo[b] thiophene-2-carboxylate from commercially available starting materials is presented.

A convenient and improved procedure for the cyanation of enamines and 1,3-dicarboxyl compounds

Buttke,Niclas

, p. 3241 - 3248 (2007/10/02)

The direct cyanation of enamines 2a-f using acylsubstituted cyanatobenzenes 1a-c and cyanatoanthraquinone 1d furnishes β-cyanoenamines 3a-f which upon hydrolysis afford the cyanoketones 4a,b. 2-Cyano-1,3-diketones 6a-c are obtained starting from compounds

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