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DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE, with the molecular formula C7H11NO4S, is a versatile chemical compound that serves as a fundamental building block in the synthesis of pharmaceuticals and agrochemicals. It is recognized for its anti-inflammatory and antioxidant properties, positioning it as a promising candidate for the development of innovative drugs. Its distinctive structure and reactivity further contribute to its utility in organic synthesis for creating a range of functionalized compounds. However, due to potential health hazards, it is crucial to handle DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE with caution, ensuring proper use and storage.

318233-97-5

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318233-97-5 Usage

Uses

Used in Pharmaceutical Industry:
DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with anti-inflammatory and antioxidant properties.
Used in Agrochemical Industry:
DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE is utilized as a building block in the creation of agrochemicals, leveraging its chemical properties to enhance the effectiveness of these products.
Used in Organic Synthesis:
DIMETHYL THIAZOLIDINE-2,4-DICARBOXYLATE is employed as a reactant in organic synthesis processes to produce a variety of functionalized compounds, capitalizing on its unique structure and reactivity.

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 academic research and scientific papers

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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