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Ethanone, 2-bromo-1-(1-methyl-1H-pyrrol-2-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65438-97-3

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65438-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65438-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65438-97:
(7*6)+(6*5)+(5*4)+(4*3)+(3*8)+(2*9)+(1*7)=153
153 % 10 = 3
So 65438-97-3 is a valid CAS Registry Number.

65438-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-(1-methylpyrrol-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-BROMO-1-(1-METHYL-1H-PYRROL-2-YL)-ETHANONE

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:65438-97-3 SDS

65438-97-3Downstream Products

65438-97-3Relevant academic research and scientific papers

ANTIBACTERIAL BENZOIC ACID DERIVATIVES

-

Page 356, (2010/02/06)

The invention provides antimicrobial agents and methods of using the agents for sterilization, sanitation, antisepsis, disinfection, and treatment of infections in mammals.

Pyrrole analogues of chloramphenicol. I. Synthesis and antibacterial activity of DL-threo-1-(1-methyl-4-nitro-pyrrole-2-yl)-2-dichloroacetamidopropane-1,3-diol

Krajewska, Dorota,Dabrowska, Marta,Jakoniuk, Piotr,Rozanski, Andrzej

, p. 213 - 221 (2007/10/03)

The seven-stage synthesis of a pyrrole analogue of chloramphenicol [IX] was described. The compound exhibits a significant antibacterial activity, over the 12-50% range of the chloramphenicol activity.

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