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1H-Pyrrole-3-carboxamide, 4-amino-1-phenyl- is a complex organic compound with the chemical formula C11H10N4O. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. The compound features a pyrrole ring with a carboxamide group at the 3-position and an amino group at the 4-position. Additionally, it has a phenyl group attached to the amino group, which contributes to its structure and potential applications. 1H-Pyrrole-3-carboxamide, 4-amino-1-phenyl- may be of interest in the fields of pharmaceuticals, materials science, and organic chemistry due to its unique structure and potential reactivity.

88796-36-5

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88796-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88796-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88796-36:
(7*8)+(6*8)+(5*7)+(4*9)+(3*6)+(2*3)+(1*6)=205
205 % 10 = 5
So 88796-36-5 is a valid CAS Registry Number.

88796-36-5SDS

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 4-amino-1-phenylpyrrole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-3-carboxamide,4-amino-1-phenyl

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:88796-36-5 SDS

88796-36-5Relevant academic research and scientific papers

On the Synthesis of 3-amino-pyrroles by Thorpe-Ziegler-Cyclization

Gewald, K.,Schaefer, H.,Bellmann, P.,Hain, U.

, p. 491 - 496 (2007/10/02)

N-Aryl and alkylaminomethylene cyanacetic acid derivatives 1 react with α-halogencarbonyl compounds 2 in the presence of potassium carbonate/sodium ethoxide to yield the substituted 3-amino-pyrroles 6.Using the same principle of cyclization pyrrole deriva

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