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357338-13-7

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357338-13-7 Usage

General Description

The chemical compound "(S)-2-(2-oxo-4-propyl-2,5-dihydro-1H-pyrrol-1-yl)butanamide" is a pyrrole derivative that contains a propyl group and a butanamide group. It is classified as a chiral compound, with the (S) configuration indicating its specific spatial arrangement. (S)-2-(2-oxo-4-propyl-2,5-dihydro-1H-pyrrol-1-yl)butanamide may have potential applications in pharmaceutical research, as pyrrole derivatives are known for their diverse biological activities, including anti-inflammatory, antibacterial, and antifungal properties. Further studies on the synthesis and properties of this compound may reveal its potential use in drug development and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 357338-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,3,3 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 357338-13:
(8*3)+(7*5)+(6*7)+(5*3)+(4*3)+(3*8)+(2*1)+(1*3)=157
157 % 10 = 7
So 357338-13-7 is a valid CAS Registry Number.

357338-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(2S)-2-(2-oxo-4-propyl-2,5-dihydro-1H-pyrrol-1-yl)butanamide

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:357338-13-7 SDS

357338-13-7Relevant articles and documents

Formal synthesis of brivaracetam: A key to construct the pyrrolidone scaffold using Pd-catalyzed oxidative cyclization and ring-closing metathesis reaction

Chavan, Subhash P.,Kawale, Sanket A.,Chavan, Prakash N.

supporting information, (2019/11/11)

A short and efficient synthetic approach for brivaracetam has been accomplished via two different routes which utilize Pd-catalyzed oxidative cyclization and ring-closing metathesis (RCM) as the key reaction. These two routes are novel, simple, scalable and rely on (E)-pent-2-en-1-ol and valeraldehyde as a commercially available starting material to yield brivaracetam with good overall yield.

CONTINUOUS PROCESS FOR PREPARING BRIVARACETAM

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Page/Page column 10, (2017/09/02)

The present invention relates to a continuous flow process for preparing brivaracetam.

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