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211682-21-2

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211682-21-2 Usage

Structure

Cyclic organic compound with a pyrrolidin-2,5-dione structure and a 1,3-dimethyl substitution at the nitrogen atom

Stereochemistry

(3S)-(9CI)

Applications

Used as a building block in organic synthesis and in the pharmaceutical industry for the development of new drugs

Potential Uses

Research and development for its unique chemical properties and potential biological activities

Handling

Should be handled with care and proper safety precautions

Check Digit Verification of cas no

The CAS Registry Mumber 211682-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,6,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 211682-21:
(8*2)+(7*1)+(6*1)+(5*6)+(4*8)+(3*2)+(2*2)+(1*1)=102
102 % 10 = 2
So 211682-21-2 is a valid CAS Registry Number.

211682-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-1,3-dimethylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:211682-21-2 SDS

211682-21-2Downstream Products

211682-21-2Relevant articles and documents

Pyrrolidinedione derivatives as antibacterial agents with a novel mode of action

Pohlmann, Jens,Lampe, Thomas,Shimada, Mitsuyuki,Nell, Peter G.,Pernerstorfer, Josef,Svenstrup, Niels,Brunner, Nina A.,Schiffer, Guido,Freiberg, Christoph

, p. 1189 - 1192 (2007/10/03)

The pseudopeptide pyrrolidinedione natural products moiramide B and andrimid represent a new class of antibiotics that target bacterial fatty acid biosynthesis. Structure-activity relationship (SAR) studies revealed a high degree of variability for the fa

SUBSTITUTED ALKYLAMIDES

-

Page/Page column 31, (2010/02/10)

The invention relates to compounds, method for producing them, pharmaceutical compositions comprising them and the use thereof in the treatment and/or prophylaxis of human or animal diseases, especially bacterial infectious diseases.

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