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318233-97-5

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318233-97-5 Usage

General Description

Dimethyl thiazolidine-2,4-dicarboxylate is a chemical compound with the molecular formula C7H11NO4S. It is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE has been reported to exhibit anti-inflammatory and antioxidant properties, making it a potential candidate for use in the development of new drugs. Its unique structure and reactivity also make it useful in organic synthesis for the production of various functionalized compounds. However, it is important to handle dimethyl thiazolidine-2,4-dicarboxylate with care, as it may pose health hazards if not used and stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 318233-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,8,2,3 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 318233-97:
(8*3)+(7*1)+(6*8)+(5*2)+(4*3)+(3*3)+(2*9)+(1*7)=135
135 % 10 = 5
So 318233-97-5 is a valid CAS Registry Number.

318233-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 1,3-thiazolidine-2,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 1,3-thiazolane-2,4-dicarboxylate

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:318233-97-5 SDS

318233-97-5Relevant articles and documents

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 (1997)

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.

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