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5025-82-1

5025-82-1

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  • N-Acetyl-Thiazolidine-4-Carboxylic Acid (Folcisteine)

    Cas No: 5025-82-1

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5025-82-1 Usage

Uses

3-Acetyl-4-thiazolidinecarboxylic acid is a reactant in the reaction of cyclic N-acyl-α-amino acids with N-(phenylmethylene)benzenesulfonamide.

Check Digit Verification of cas no

The CAS Registry Mumber 5025-82-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5025-82:
(6*5)+(5*0)+(4*2)+(3*5)+(2*8)+(1*2)=71
71 % 10 = 1
So 5025-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO3S/c1-4(8)7-3-11-2-5(7)6(9)10/h5H,2-3H2,1H3,(H,9,10)

5025-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Acetylthiazolidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Acetyl-thiazolidine-4-carboxylic acid

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:5025-82-1 SDS

5025-82-1Downstream Products

5025-82-1Relevant articles and documents

PROCESS FOR OBTAINING MIXTURES OF 4-CARBOXY-1,3-THIAZOLIDINIUM CARBOXYLATE AND N-ACYL-1,3-THIAZOLIDIN-4-CARBOXYLIC ACID

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Page/Page column 8-9; 10, (2009/06/27)

The present invention relates to a process for obtaining in a single synthesis stage mixtures of 4-carboxy-1,3-thiazolidium carboxylate and N-acyl-1, 3-thiazolidin-4- carboxylic acids from 1,3-thiazolidin-4-carboxylic acids and derivatives of carboxylic acids, which has the following advantages: use of environmentally friendly solvents, lower energy consumption, lower consumption of acylating reagents, which allows the corresponding mixtures to be obtained with suitable characteristics and specifications, ease of recovery from the reaction medium and high yields.

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