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Methanimidamide, N-(3-cyano-4-phenyl-1H-pyrrol-2-yl)-, also known as 2-(3-cyano-4-phenyl-1H-pyrrol-2-yl)-N-hydroxyacetamide, is a complex organic compound with the molecular formula C12H10N4O2. It is characterized by a pyrrole ring with a cyano group at position 3 and a phenyl group at position 4, connected to an acetamide group through a nitrogen atom. Methanimidamide,N-(3-cyano-4-phenyl-1H-pyrrol-2-yl)- is of interest in the field of organic chemistry and may have potential applications in the development of new pharmaceuticals or materials due to its unique structure and properties.

1593-20-0

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1593-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1593-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1593-20:
(6*1)+(5*5)+(4*9)+(3*3)+(2*2)+(1*0)=80
80 % 10 = 0
So 1593-20-0 is a valid CAS Registry Number.

1593-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(3-cyano-4-phenyl-1H-pyrrol-2-yl)methanimidamide

1.2 Other means of identification

Product number -
Other names 1-(Chlorodifluoromethyl)-2-fluorobenzene

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 -
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More Details:1593-20-0 SDS

1593-20-0Relevant academic research and scientific papers

7-alkyl- and 7-cycloalkyl-5-aryl-pyrrolo[2,3-d]pyrimidines - Potent inhibitors of the tyrosine kinase c-Src

Widler, Leo,Green, Jonathan,Missbach, Martin,Susa, Mira,Altmann, Eva

, p. 849 - 852 (2007/10/03)

7-Substituted-5-aryl-pyrrolo[2,3-d]pyrimidines have been prepared starting from α-bromoacetophenones. These compounds represent a novel class of potent inhibitors of the tyrosine kinase pp60c-Src with good specificity towards other tyrosine kinases (EGF-R, v-Abl).

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