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156371-85-6

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156371-85-6 Usage

General Description

(S)-3-Mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester is a chemical compound that belongs to the class of pyrrolidine carboxylic acid esters. It is a derivative of a sulfur-containing amino acid and is commonly used in organic chemistry research and drug development. (S)-3-Mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester is usually synthesized for its potential use as a building block in the production of pharmaceuticals and other organic compounds. The tert-butyl ester group in the molecule provides stability and protection for the carboxylic acid functionality, making it a versatile intermediate in organic synthesis. This chemical compound has potential applications in the fields of medicinal chemistry, drug discovery, and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 156371-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,7 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156371-85:
(8*1)+(7*5)+(6*6)+(5*3)+(4*7)+(3*1)+(2*8)+(1*5)=146
146 % 10 = 6
So 156371-85-6 is a valid CAS Registry Number.

156371-85-6SDS

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 tert-butyl (3S)-3-sulfanylpyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (S)-3-Mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester

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:156371-85-6 SDS

156371-85-6Downstream Products

156371-85-6Relevant articles and documents

BROAD-SPECTRUM CARBAPENEMS

-

, (2019/12/25)

The present disclosure provides broad-spectrum carbapenem derivatives and pharmaceutical compositions useful in the treatment of bacterial infections and methods for treating such infections using such derivatives and/or compositions.

N-SUBSTITUTED SATURATED HETEROCYCLIC SULFONE COMPOUNDS WITH CB2 RECEPTOR AGONISTIC ACTIVITY

-

Page/Page column 81, (2010/08/08)

This invention relates to compounds of formula (I) or a pharmaceutically acceptable salt thereof, wherein X, R1, R2,R3, R4, R5, R6, R7, k, m, n, p, q, r and s are each as described herein, and compositions containing such compounds, and the use of such compounds in the treatment of a condition mediated by CB2 receptor activity.

Constrained (l-)-S-adenosyl-l-homocysteine (SAH) analogues as DNA methyltransferase inhibitors

Isakovic, Ljubomir,Saavedra, Oscar M.,Llewellyn, David B.,Claridge, Stephen,Zhan, Lijie,Bernstein, Naomy,Vaisburg, Arkadii,Elowe, Nadine,Petschner, Andrea J.,Rahil, Jubrail,Beaulieu, Norman,Gauthier, France,MacLeod, A. Robert,Delorme, Daniel,Besterman, Jeffrey M.,Wahhab, Amal

scheme or table, p. 2742 - 2746 (2010/03/03)

Potent SAH analogues with constrained homocysteine units have been designed and synthesized as inhibitors of human DNMT enzymes. The five membered (2S,4S)-4-mercaptopyrrolidine-2-carboxylic acid, in 1a, was a good replacement for homocysteine, while the corresponding six-member counterpart was less active. Further optimization of 1a, changed the selectivity profile of these inhibitors. A Chloro substituent at the 2-position of 1a, compound 1d, retained potency against DNMT1, while N6 alkylation, compound 7a, conserved DNMT3b2 activity. The concomitant substitutions of 1a at both 2- and N6 positions reduced activity against both enzymes.

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