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55234-12-3

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55234-12-3 Usage

Description

3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid, also known as thiamine tetramethylthiazolium hydrochloride, is a synthetic organic compound derived from thiamine (vitamin B1). It is a thiazole derivative with a molecular formula of C11H17NO2S and a molecular weight of 231.33 g/mol. 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid is recognized for its reactivity with various organic compounds, establishing it as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other industrial products. Despite its utility, its application is cautiously managed due to inherent potential hazards and risks.

Uses

Used in Pharmaceutical Industry:
3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid serves as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to react with a range of organic compounds makes it instrumental in the development of new drugs and medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid is utilized as a precursor in the production of pesticides and other agrochemicals. Its versatility in chemical reactions contributes to the creation of effective and targeted pest control solutions.
Used in Chemical Synthesis:
3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid is employed as a reagent in chemical synthesis across various industries. Its capacity to engage in diverse chemical reactions allows for the production of a wide array of industrial products, from specialty chemicals to advanced materials.
Used in Research and Development:
3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid is also used in research and development settings to explore new chemical reactions and syntheses. Its reactivity provides a valuable tool for scientists to investigate novel pathways and mechanisms in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 55234-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,3 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55234-12:
(7*5)+(6*5)+(5*2)+(4*3)+(3*4)+(2*1)+(1*2)=103
103 % 10 = 3
So 55234-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO3S/c1-8(2)6(7(12)13)10(5-11)9(3,4)14-8/h5-6H,1-4H3,(H,12,13)

55234-12-3SDS

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 3-formyl-2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Formyl-2,2,5,5-tetramethyl-thiazolidin-4-carbonsaeure

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:55234-12-3 SDS

55234-12-3Relevant articles and documents

DUAL ACTION NITRIC OXIDE DONORS AND THEIR USE AS ANTIMICROBIAL AGENTS

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Page/Page column 75, (2014/05/24)

The present invention relates generally to conjugates comprising a nitric oxide donor and an acyl homoserine lactone, fimbrolide, fimbrolide derivative, dihydropyrrolone or indole, and to the use of such conjugates as antimicrobial agents.

Process for the splitting of the racemate of d-1-phenylpropanolamine

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, (2008/06/13)

The d,1-phenylpropanolamine(norephedrine) racemate is split with optically active thiazolidine-4-carboxylic acids of the formula: EQU1 where R1 and R2 are both methyl or are joined together to form the pentamethylene group.

Process for the resolution of D,L-penicillamine and salts formed during said process

-

, (2008/06/13)

D,L-penicillamine is separated into its antipodes employing optically active threo-1-(p-nitrophenyl)-2-aminopropanediol-1,3.

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