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1-Methylpyrrole-2-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34884-10-1

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34884-10-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 107, p. 5279, 1985 DOI: 10.1021/ja00304a045Tetrahedron Letters, 34, p. 141, 1993 DOI: 10.1016/S0040-4039(00)60078-3

Check Digit Verification of cas no

The CAS Registry Mumber 34884-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34884-10:
(7*3)+(6*4)+(5*8)+(4*8)+(3*4)+(2*1)+(1*0)=131
131 % 10 = 1
So 34884-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2/c1-8-4-2-3-6(8)5-7/h2-4H,1H3

34884-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methylpyrrole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-cyano-N-methylpyrrole

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:34884-10-1 SDS

34884-10-1Relevant academic research and scientific papers

Substituted thiazole derivatives useful as platelet aggregation inhibitors

-

, (2008/06/13)

This invention relates to substituted thiazole derivatives of the following general formula, the substituent groups of which are as defined herein: STR1 These compounds are useful as inhibitors of platelet aggregation and inhibitors of adhesion molecules and may be provided in pharmaceutical compositions and in methods of treating reperfusion thrombosis injury in patients.

STUDIES ON DIMETHYLHYDRAZONES OF HETEROARYL ALDEHYDES. THE REACTIVITY OF 2-FORMYLFURAN, 2-FORMYLTHIOPHENE AND 1-METHYL-2-FORMYLPYRROLE N,N-DIMETHYLHYDRAZONES WITH METHYL PROPIOLATE AND DIETHYL AZODICARBOXYLATE

Abarca, Belen,Ballesteros, Rafael,Gonzalez, Eugenia,Sancho, Pedro,Sepulveda, Jose,Soriano, Concepcion

, p. 1811 - 1817 (2007/10/02)

The title hydrazones react with methyl propiolate giving the new 2-heteroarylpyridines (4, 5 and 6).The reaction with diethyl azodicarboxylate gives 1:1 Michael adducts except with formylthiophene hydrazone that gives the compound (14) a novel type of 1:1 adduct.

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