261527-23-5

Basic information

• Product Name: Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester
• Synonyms: Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester
• CAS NO: 261527-23-5
• Molecular Weight: 279.403
• Mol File: 261527-23-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester(261527-23-5)
• EPA Substance Registry System: Dimethylthiocarbamic acid S-(2-tert-butyl-4-formyl-5-methylphenyl) ester(261527-23-5)

Safety Data

• Hazardous Substances Data: 261527-23-5(Hazardous Substances Data)

Upstream product

• 261527-22-4 Dimethylthiocarbamic acid O-(2-tert-butyl-4-formyl-5-methylphenyl) ester 
• 16805-16-6 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde 

Downstream Products

• 261527-24-6 Dimethylthiocarbamic acid S-(2-tert-butyl-4-hydroxymethyl-5-methylphenyl) ester 
• 207737-06-2 toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxymethyl-5-methyl-phenyl) ester 
• 207737-05-1 2-tert-Butyl-4-hydroxymethyl-5-methylthiophenol 

Relevant articles and documents

HIV protease inhibitors

The present invention relates to novel dihydropyrones with tethered heterocycles having improved pharmacologic properties which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The dihydropyrones are useful in the development of therapies for the treatment of viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of the dihydropyrones and intermediates useful in the preparation of the final compounds.

A continuous procedure for preparation of para functionalized aromatic thiols using Newman-Kwart chemistry

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