197906-36-8

Basic information

• Product Name: [2-Methoxy-5-methyl-3-(2-thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone
• Synonyms: [2-Methoxy-5-methyl-3-(2-thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone
• CAS NO: 197906-36-8
• Molecular Weight: 412.579
• Mol File: 197906-36-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [2-Methoxy-5-methyl-3-(2-thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [2-Methoxy-5-methyl-3-(2-thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone(197906-36-8)
• EPA Substance Registry System: [2-Methoxy-5-methyl-3-(2-thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone(197906-36-8)

Safety Data

• Hazardous Substances Data: 197906-36-8(Hazardous Substances Data)

Upstream product

• 197906-32-4 2-methoxy-5-methylbenzene-1,3-dicarboxylic acid 
• 6327-85-1 2,6-bis(hydroxymethyl)-4-methyl-anisole 
• 106-44-5 p-cresol 
• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 
• 134469-06-0 thiazolidine-2-thione 
• 197906-33-5 2-methoxy-5-methylisophthaloyl dichloride 

Relevant articles and documents

Synthesis of macrocyclic polyhydroxy tetralactams derived from L-tartaric acid and β-hydroxyglutaric acid

The synthesis of new 16-, 18-, 19- or 20-membered secondary tetralactams with L-tartaric acid or β-hydroxyglutaric acid moieties is investigated. The stepwise synthesis with an intermediate diamide diamine provides overall good yields (30-55%) compared with other processes using an intermediate diamide diacid or direct macrocyclization. This synthetic pathway leads to symmetrical or unsymmetrical polyhydroxytetralactams with variable hydroxyl group number. Use of mild acylating agents in this approach allows to avoid the protection-deprotection steps of hydroxyl groups.