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7126-47-8

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7126-47-8 Usage

Structure

Pyrrole ring with an amide group and two methyl groups attached to the nitrogen atom

Classification

Derivative of pyrrole, belongs to the class of carboxamide compounds

Usage

Building block in the synthesis of various pharmaceuticals and organic compounds

Potential activities

May have biological and pharmacological activities, making it of interest in drug discovery and development

Further research needed

To fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7126-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7126-47:
(6*7)+(5*1)+(4*2)+(3*6)+(2*4)+(1*7)=88
88 % 10 = 8
So 7126-47-8 is a valid CAS Registry Number.

7126-47-8SDS

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 N,N-Dimethyl-1H-pyrrole-2-carboxamide

1.2 Other means of identification

Product number -
Other names pyrrole-2-carboxylic acid N,N-dimethylamide

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:7126-47-8 SDS

7126-47-8Relevant articles and documents

Substrate Controlled Regioselective Bromination of Acylated Pyrroles Using Tetrabutylammonium Tribromide (TBABr3)

Gao, Shuang,Bethel, Travis K.,Kakeshpour, Tayeb,Hubbell, Grace E.,Jackson, James E.,Tepe, Jetze J.

, p. 9250 - 9255 (2018/07/15)

Electrophilic bromination of pyrroles bearing carbonyl substituents at C-2 typically results in a mixture of the 4- and 5-brominated species, generally favoring the 4-position. Herein, we describe a substrate-controlled regioselective bromination in which

3-Substituted-5,6,7,8-tetrahydropyrrolo[1,2-a]-pyridine-and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]-azepine carboxylic acid derivatives useful as blood platelet aggregation inhibitors

-

, (2008/06/13)

Novel 3-substituted-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylic acid and 3-substituted-6,7,8,9-tetrahydro[1,2-a]azepine-9-carboxylic acid compounds represented by the formula STR1 and the pharmaceutically acceptable, non-toxic esters and salts t

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