55234-12-3

Basic information

• Product Name: 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid
• Synonyms: 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid;3-Formyl-2,2,5,5-tetramethyl-4-thiazolidinecarboxylic acid;Einecs 259-542-3;3-Formyl-2,2,5,5-tetramethyl-1,3-thiazolane-4-carboxylic acid, 4-Carboxy-3-formyl-2,2,5,5-tetramethyl-1,3-thiazolidine;3-Formyl-2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylic acid
• CAS NO: 55234-12-3
• Molecular Formula: C₉H₁₅NO₃S
• Molecular Weight: 217.2853
• EINECS: 259-542-3
• Mol File: 55234-12-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid(55234-12-3)
• EPA Substance Registry System: 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid(55234-12-3)

Safety Data

• Hazardous Substances Data: 55234-12-3(Hazardous Substances Data)

Usage

General Description

3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid, also known as thiamine tetramethylthiazolium hydrochloride, is a synthetic organic compound that is derived from thiamine (vitamin B1). It is a derivative of thiazole and is commonly used as a reagent in chemical synthesis. 3-formyl-2,2,5,5-tetramethylthiazolidine-4-carboxylic acid has a molecular formula of C11H17NO2S and a molecular weight of 231.33 g/mol. It is known for its ability to react with a variety of other organic compounds, making it a versatile building block in the production of pharmaceuticals, agrochemicals, and other industrial products. However, its use is strictly controlled due to its potential hazards and risks.

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)

Upstream product

• 64-18-6 formic acid 
• 141-53-7 sodium formate 
• 58131-62-7 2,2,5,5-tetramethyl thiazolidine-4-carboxylic acid 
• 33078-43-2 2,2,5,5-tetramethyl thiazolidine-4-carboxylic acid hydrochloride 
• 22572-05-0 penicillamine hydrochloride 

Downstream Products

• 101496-50-8 3-formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid anilide 
• 40626-23-1 3-formyl-2,2,5,5-tetramethylthiazolidine-4S-carboxylic acid 
• 40626-24-2 (R)-3-formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid 
• 101396-91-2 N-(3-chloro-2-hydroxypropyl)trimethylammonium chloride 
• 134020-09-0 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid (2R,3S,5R)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-trityloxymethyl-tetrahydro-furan-3-yl ester 
• 85929-76-6 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid benzylamide 
• 85929-77-7 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid (1-phenyl-ethyl)-amide 
• 85929-74-4 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid N'-phenyl-hydrazide 
• 85929-81-3 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carbothioic acid S-(2,4,5-trichloro-phenyl) ester 
• 85929-75-5 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid cyclohexylamide 

Relevant articles and documents

DUAL ACTION NITRIC OXIDE DONORS AND THEIR USE AS ANTIMICROBIAL AGENTS

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

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

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