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117186-74-0

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117186-74-0 Usage

General Description

The chemical compound (S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide is a pyrrolidine derivative with a benzoylphenyl group attached. It is a chiral compound, meaning it has a non-superimposable mirror image, and the (S) prefix indicates that it has a specific spatial arrangement of atoms. (S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide has potential therapeutic applications, particularly in the field of medicinal chemistry. It may be used in the development of pharmaceutical drugs for various purposes, such as in the treatment of neurological disorders, pain management, or as a potential antiviral agent. Further research and testing are required to fully understand the potential uses and effects of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 117186-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,8 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 117186-74:
(8*1)+(7*1)+(6*7)+(5*1)+(4*8)+(3*6)+(2*7)+(1*4)=130
130 % 10 = 0
So 117186-74-0 is a valid CAS Registry Number.

117186-74-0SDS

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 (2S)-N-(2-benzoylphenyl)pyrrolidine-2-carboxamide

1.2 Other means of identification

Product number -
Other names FD1109

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:117186-74-0 SDS

117186-74-0Relevant articles and documents

Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions

Legerén, Loreto,Domínguez, Domingo

experimental part, p. 2718 - 2722 (2010/05/02)

The efficiency of a cyclodehydration reaction leading to benzodiazepinones is markedly improved by N-methylation of the amide link connecting the nucleophile and the electrophile, which is attributed to its favouring both the more reactive E-rotamer and the exit of the leaving group.

ATTACHMENT OF THE CHIRAL REAGENT (S)-2N(N'-BENZYLPROLYL)-AMINOBENZOPHENONE TO A POLYMERIC CARRIER

Nosova, N. A.,Lysova, L. A.,Ryzhov, M. T.,Vauchskii, Yu. P.,Istomina, V. P.,Anodina, N. M.

, p. 1433 - 1436 (2007/10/02)

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