207737-06-2

Basic information

• Product Name: toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester
• Synonyms: toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester
• CAS NO: 207737-06-2
• Molecular Weight: 364.53
• Mol File: 207737-06-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester(207737-06-2)
• EPA Substance Registry System: toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester(207737-06-2)

Safety Data

• Hazardous Substances Data: 207737-06-2(Hazardous Substances Data)

Upstream product

• 88-60-8 2-tert-Butyl-5-methylphenol 
• 261527-24-6 Dimethylthiocarbamic acid S-(2-tert-butyl-4-hydroxymethyl-5-methylphenyl) ester 
• 261527-22-4 Dimethylthiocarbamic acid O-(2-tert-butyl-4-formyl-5-methylphenyl) ester 
• 261527-23-5 Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester 
• 16805-16-6 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde 
• 1950-69-2 toluene-p-sulfonyl bromide 
• 207737-05-1 2-tert-Butyl-4-hydroxymethyl-5-methylthiophenol 
• 207737-01-7 5-tert-Butyl-4-(2-methoxy-ethoxymethoxy)-2-methyl-benzoic acid 
• 207737-03-9 5-tert-Butyl-4-dimethylthiocarbamoyloxy-2-methyl-benzoic acid methyl ester 
• 207737-04-0 5-tert-Butyl-4-dimethylcarbamoylsulfanyl-2-methyl-benzoic acid methyl ester 
• 207737-00-6 1-Bromo-5-tert-butyl-4-(2-methoxy-ethoxymethoxy)-2-methyl-benzene 
• 207737-02-8 5-tert-Butyl-4-hydroxy-2-methyl-benzoic acid methyl ester 
• 51345-97-2 4-Bromo-2-tert-butyl-5-methyl-phenol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 197915-45-0 3-(2-tert-Butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-6-cyclohexyl-4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-5,6-dihydro-pyran-2-one 
• 207736-05-8 6-[2-(4-Amino-phenyl)-ethyl]-3-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-isopropyl-5,6-dihydro-pyran-2-one 
• 197915-46-1 3-[2-tert-Butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl]-4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-6-isopropyl-5,6-dihydro-pyran-2-one 
• 197915-37-0 6-[2-(4-aminophenyl)ethyl]-3-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-phenyl-5,6-dihydro-pyran-2-one 
• 197915-35-8 3-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-6-phenyl-5,6-dihydro-pyran-2-one 
• 197915-36-9 3-(2-tert-Butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-[2-(3-hydroxy-phenyl)-ethyl]-6-phenyl-5,6-dihydro-pyran-2-one 
• 197915-28-9 3-(tert-Butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-phenethyl-6-phenyl-5,6-dihydro-pyran-2-one 
• 197915-46-1 3-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6-[2-(4-hydroxy-phenyl)ethyl]-6-isopropyl-5,6-dihydro-pyran-2-one 

Relevant articles and documents

Methods of making dihydropyrone HIV protease inhibitors

The present invention relates to methods of making dihydropyrone HIV inhibitors.

Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones as HIV-1 protease inhibitors: the profound effect of polarity on antiviral activity.

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