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915205-76-4

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915205-76-4 Usage

Description

(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is a chemical compound with the molecular formula C19H23NO3. It is a derivative of pyrrolidine, an organic compound with a five-membered ring containing one nitrogen atom. This specific compound has a hydroxyl group and a carboxylic acid group attached to the pyrrolidine ring, as well as two benzyl groups bonded to the amide nitrogen. It is commonly used as a building block in organic synthesis and can be found in research and pharmaceutical applications.

Uses

Used in Organic Synthesis:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and properties make it a valuable component in the synthesis of new molecules.
Used in Research Applications:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in research applications to study its properties and potential uses. Its unique structure allows researchers to explore its potential in various fields, such as drug development and material science.
Used in Pharmaceutical Applications:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in pharmaceutical applications for the development of new drugs. Its unique structure and properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Drug Development:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in drug development to create new pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of innovative drugs with potential therapeutic benefits.
Used in Material Science:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in material science to develop new materials with unique properties. Its structure and properties make it a promising candidate for the creation of innovative materials with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 915205-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,2,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 915205-76:
(8*9)+(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*7)+(1*6)=154
154 % 10 = 4
So 915205-76-4 is a valid CAS Registry Number.

915205-76-4 Well-known Company Product Price

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  • Aldrich

  • (671290)  (2S,4R)-4-Hydroxypyrrolidine-2-carboxylicaciddibenzylamide  99% (HPLC)

  • 915205-76-4

  • 671290-100MG

  • 464.49CNY

  • Detail
  • Aldrich

  • (671290)  (2S,4R)-4-Hydroxypyrrolidine-2-carboxylicaciddibenzylamide  99% (HPLC)

  • 915205-76-4

  • 671290-500MG

  • 1,845.09CNY

  • Detail

915205-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4R)-N,N-dibenzyl-4-hydroxypyrrolidine-2-carboxamide

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:915205-76-4 SDS

915205-76-4Downstream Products

915205-76-4Relevant articles and documents

An enantioselective Biginelli reaction catalyzed by a simple chiral secondary amine and achiral Bronsted acid by a dual-activation route

Xin, Junguo,Chang, Lu,Hou, Zongrui,Shang, Deju,Liu, Xiaohua,Feng, Xiaoming

supporting information; experimental part, p. 3177 - 3181 (2009/04/11)

An enantioselective Biginelli reaction that proceeds by a dual-activation route has been developed by using a combined catalyst of a readily available trans-4-hydroxyproline-derived secondary amine and a Bronsted acid. Aromatic, heteroaromatic, and fusedr

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