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(2Z)-2-cyano-2-[1-(cyanomethyl)pyrrolidin-2-ylidene]ethanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91417-83-3

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91417-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91417-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,1 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91417-83:
(7*9)+(6*1)+(5*4)+(4*1)+(3*7)+(2*8)+(1*3)=133
133 % 10 = 3
So 91417-83-3 is a valid CAS Registry Number.

91417-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-2-cyano-2-[1-(cyanomethyl)pyrrolidin-2-ylidene]acetamide

1.2 Other means of identification

Product number -
Other names LS-8710

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:91417-83-3 SDS

91417-83-3Downstream Products

91417-83-3Relevant academic research and scientific papers

ACETALS OF LACTAMS AND ACID AMIDES. 50. 1-CYANOMETHYLPYRROLID-2-ONE DIETHYLACETAL IN THE SYNTHESIS OF DERIVATIVES OF PYRROLOPYRROLES

Kadushkin, A. V.,Stezhko, T. V.,Solov'eva, N. P.,Granik, V. G.

, p. 1297 - 1301 (2007/10/02)

We have synthesized a series of enamines - derivatives of 1-cyanomethyl-2-methylenepyrrolidine - by reaction of 1-cyanomethylpyrrolid-2-one diethylacetal with compounds having a reactive methylene link.The enamines undergo a Thorpe-Ziegler cyclization in the presence of bases with the formation of pyrrolopyrrole derivatives.The configuration of the enamines obtained were studied using PMR spectroscopy.

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