99972-65-3

Basic information

• Product Name: AKOS B018316
• Synonyms: AKOS B018316;CHEMBRDG-BB 3018316;ART-CHEM-BB B018316;(5E)-5-(2-hydroxy-3-methoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one;Albb-009168;(5E)-5-(2-hydroxy-3-methoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one(SALTDATA: FREE);(5Z)-5-[(2-hydroxy-3-methoxyphenyl)methylene]-2-thioxo-4-thiazolidinone;(5Z)-5-[(2-hydroxy-3-methoxy-phenyl)methylene]-2-thioxo-thiazolidin-4-one
• CAS NO: 99972-65-3
• Molecular Formula: C₁₁H₉NO₃S₂
• Molecular Weight: 267.32
• Mol File: 99972-65-3.mol

Chemical Properties

• Boiling Point: 442.3°C at 760 mmHg
• Flash Point: 221.3°C
• Appearance: /
• Density: 1.53g/cm³
• Vapor Pressure: 1.96E-08mmHg at 25°C
• Refractive Index: 1.735
• CAS DataBase Reference: AKOS B018316(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS B018316(99972-65-3)
• EPA Substance Registry System: AKOS B018316(99972-65-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 99972-65-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
AKOS B018316 is used as a precursor for the production of various pharmaceuticals due to its versatile chemical properties.
Used in Dye Industry:
AKOS B018316 is used as a precursor in the production of dyes, contributing to the coloration of various products.
Used in Flavoring and Fragrance Industry:
AKOS B018316 is used as a flavoring agent in the manufacturing of cough syrups and other medicinal products, as well as in the production of fragrances, due to its characteristic smoky odor.
Used in Food Industry:
AKOS B018316 is used as a food flavoring agent, enhancing the taste and aroma of various food products.
Used in Organic Synthesis:
AKOS B018316 has potential applications in organic synthesis, serving as a valuable intermediate in the synthesis of other organic compounds.
Used as a Reagent in Chemical Reactions:
AKOS B018316 is used as a reagent in various chemical reactions, facilitating specific transformations and processes in the chemical industry.

InChI:InChI=1/C11H9NO3S2/c1-15-7-4-2-3-6(9(7)13)5-8-10(14)12-11(16)17-8/h2-5,13H,1H3,(H,12,14,16)/b8-5+

Upstream product

• 141-84-4 2-thioxo-4-thiazolidinone 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Downstream Products

• 521973-03-5 5-((Z)-4-hydroxy-3-methoxybenzylidene)-2-methylmercapto-4-thiazolidinone 
• 521973-11-5 2-(5-(4-hydroxy-3-methoxybenzylidene)-4-oxo-thiazolidin-2-ylideneamino)benzoic acid 
• 521973-15-9 2-(5-(2-hydroxy-3-methoxybenzylidene)-4-oxo-thiazolidin-2-ylideneamino)-4,5-dimethoxybenzoic acid 
• 1352457-87-4 5-((Z)-(2-hydroxy-3-methoxybenzylidene))-3-β-D-galactopyranosyl-2-thioxo-4-thiazolidinone 
• 1352457-77-2 C₂₅H₂₇NO₁₂S₂ 
• 1352457-76-1 5-((Z)-(2-hydroxy-3-methoxybenzylidene))-3-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)-2-thioxo-4-thiazolidinone 

Relevant articles and documents

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N-ribosylation and N-mannosylation compounds have a great role in compounds activity as anticancer. The reaction of 2-thioxo-4-thiazolidinone (rhodanine) derivatives, as aglycon part, was done with ribofuranose and mannopyranose sugars (glycone part) foll

A new approach for the N- and S-galactosylation of 5-arylidene-2-thioxo-4- thiazolidinones

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A convenient synthesis of 2-arylidene-5H-thiazolo[2,3-b]quinazoline-3,5[2H]-diones and their benzoquinazoline derivatives

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