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(2S,3R)-CIS-3-METHYL-L-PROLINE ETHYL ESTER is a chemical compound derived from proline, an essential amino acid in the human body. It is a specific stereoisomer, with the (2S,3R) configuration indicating the arrangement of atoms within the molecule. The presence of an ethyl ester group signifies that an ethyl group is attached to the carboxyl group of the proline molecule. This unique structure and properties may lend itself to potential applications in pharmaceuticals or as a building block in organic synthesis.

186586-71-0

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186586-71-0 Usage

Uses

Used in Pharmaceutical Industry:
(2S,3R)-CIS-3-METHYL-L-PROLINE ETHYL ESTER is used as a pharmaceutical intermediate for the development of drugs targeting various medical conditions. Its unique stereochemistry and functional groups may contribute to the design of novel therapeutic agents with improved efficacy and selectivity.
Used in Organic Synthesis:
(2S,3R)-CIS-3-METHYL-L-PROLINE ETHYL ESTER is used as a building block in organic synthesis for the creation of complex organic molecules. Its distinct structure allows for the synthesis of a wide range of compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 186586-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,5,8 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 186586-71:
(8*1)+(7*8)+(6*6)+(5*5)+(4*8)+(3*6)+(2*7)+(1*1)=190
190 % 10 = 0
So 186586-71-0 is a valid CAS Registry Number.

186586-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-CIS-3-METHYL-L-PROLINE ETHYL ESTER

1.2 Other means of identification

Product number -
Other names L-Proline,3-methyl-,ethyl ester,(3R)-(9CI)

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:186586-71-0 SDS

186586-71-0Downstream Products

186586-71-0Relevant academic research and scientific papers

New strategy for the synthesis of 3-substituted prolines

Karoyan, Philippe,Chassaing, Gerard

, p. 85 - 88 (2007/10/03)

Ring formation involving a 5-exo trig cyclization between a zinc enolate and a non activated double bond led to cis diastereoisomer of 3-substituted prolines. This cyclization was achieved with transfer of chirality onto the C-2 carbon when nitrogen was protected by an α-methylbenzyl group. Reprotonation of the lithium enolate of cis derivative yielded the trans diastereoisomer.

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