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(R)-1-Cbz-2-pyrrolidineacetic acid, also known as (R)-CPPA, is a chemical compound derived from the amino acid proline with potential pharmaceutical applications. It is commonly used as a building block in the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and properties.

61350-64-9

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61350-64-9 Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-Cbz-2-pyrrolidineacetic acid is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and properties make it suitable for the development of drugs for the treatment of various medical conditions, including neurological disorders and cancer.
Used in Enzyme Inhibition:
(R)-1-Cbz-2-pyrrolidineacetic acid is used as an inhibitor of enzymes involved in the biosynthesis of fatty acids and cholesterol. Its potential as an enzyme inhibitor makes it a promising candidate for the development of new therapeutic agents.
Further research and development of (R)-1-Cbz-2-pyrrolidineacetic acid may lead to the discovery of novel drug candidates with important medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 61350-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,5 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61350-64:
(7*6)+(6*1)+(5*3)+(4*5)+(3*0)+(2*6)+(1*4)=99
99 % 10 = 9
So 61350-64-9 is a valid CAS Registry Number.

61350-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-{1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}acetic acid

1.2 Other means of identification

Product number -
Other names 2-[(2R)-1-phenylmethoxycarbonylpyrrolidin-2-yl]acetic acid

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:61350-64-9 SDS

61350-64-9Relevant academic research and scientific papers

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

Carlson, Erik C.,Rathbone, Lauren K.,Yang, Hua,Collett, Nathan D.,Carter, Rich G.

, p. 5155 - 5158 (2008/09/21)

(Chemical Equation Presented) An improved protocol for the construction of enantioenriched pyrrolidine, indoline, and piperidine rings using an organocatalyzed, intramolecular heteroatom Michael addition is described. Application to the enantioselective synthesis of homoproline, homopipecolic acid, and pelletierine has been accomplished.

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