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60667-24-5

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60667-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60667-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60667-24:
(7*6)+(6*0)+(5*6)+(4*6)+(3*7)+(2*2)+(1*4)=125
125 % 10 = 5
So 60667-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2S/c1-8-5(7)4-2-9-3-6-4/h4,6H,2-3H2,1H3

60667-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 1,3-thiazolidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names solaskil

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:60667-24-5 SDS

60667-24-5Relevant articles and documents

Bicyclic modulators of androgen receptor function

-

, (2008/06/13)

The invention provides compounds of the formula I wherein the substitutents are as described herein. Further provided are methods of using such compounds for the treatment of nuclear hormone receptor-associated conditions, such as age related diseases, for example sarcopenia, and also provided are pharmaceutical compositions containing such compounds.

3-Aminoacetylthiazolidine-4-carboxylate Esters and their 1-Thia-4-azaspiro[4.5]decane-3-carboxylate Derivatives. Synthesis and Stereochemical Properties

Pellegrini,Refouvelet,Dachet,Rouland,Robert

, p. 1685 - 1691 (2007/10/03)

Dimethyl thiazolidine-2,4-dicarboxylate 2 and ethyl 1-thia-4-azaspiro[4.5]decane-3-carboxylates 3-5 were obtained as a diastereoisomeric mixture while their 3-aminoacetyl derivatives were isolated in only one isomeric form. These reactions of N-acylation were stereoselective, which can be explained by an interconversion of the diastereoisomers via a seco intermediate. The 1H nmr analysis of amides 6 and 11 exhibited the presence of both cis and irons amide bond conformations, whereas only one cis conformation was observed for spiro amides 8-10 and 13-15.

Tetrapeptide analog of TRH

-

, (2008/06/13)

A novel tetrapeptide L-2-ketopiperidine-6-carbonyl-L-histidyl-L-thiazolidine-4-carbonyl-β-alanin-amide, (L-Kpc-L-His-L-Tca-β-ala-NH2), is a stimulant of the central nervous system. It is preparable by standard peptide synthetic procedures.

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