92651-21-3

Basic information

• Product Name: Acetic acid (3S,5S)-3,4,5-triacetoxy-1-chlorocarbonyl-cyclohexyl ester
• CAS NO: 92651-21-3
• Molecular Weight: 378.763
• Mol File: 92651-21-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Acetic acid (3S,5S)-3,4,5-triacetoxy-1-chlorocarbonyl-cyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (3S,5S)-3,4,5-triacetoxy-1-chlorocarbonyl-cyclohexyl ester(92651-21-3)
• EPA Substance Registry System: Acetic acid (3S,5S)-3,4,5-triacetoxy-1-chlorocarbonyl-cyclohexyl ester(92651-21-3)

Safety Data

• Hazardous Substances Data: 92651-21-3(Hazardous Substances Data)

Upstream product

• 23804-28-6 (-)-1,3,4,5-Tetra-O-acetylquinic acid 
• 77-95-2 D-(-)-quinic acid 
• 32469-24-2 (1R,3R,4R,5R)-(-)-quinic acid tetraacetate 

Downstream Products

• 24367-44-0 2-(2-tert-butyldisulfanyl)pyridine 
• 92822-52-1 2-((3S,5S)-1,3,4,5-Tetraacetoxy-cyclohexylmethyl)-acrylic acid ethyl ester 
• 860812-21-1 (S)-2-[((3R,5R)-1,3,4,5-Tetraacetoxy-cyclohexanecarbonyl)-amino]-pentanedioic acid dibenzyl ester 
• 860812-22-2 (S)-2-[((3R,5R)-1,3,4,5-Tetraacetoxy-cyclohexanecarbonyl)-amino]-propionic acid benzyl ester 
• 860812-23-3 (2S,3S)-3-Methyl-2-[((3R,5R)-1,3,4,5-tetraacetoxy-cyclohexanecarbonyl)-amino]-pentanoic acid benzyl ester 
• 860812-25-5 (S)-3-tert-Butoxy-2-[((3R,5R)-1,3,4,5-tetraacetoxy-cyclohexanecarbonyl)-amino]-propionic acid methyl ester 
• 860812-24-4 (2S,3R)-3-tert-Butoxy-2-[((3R,5R)-1,3,4,5-tetraacetoxy-cyclohexanecarbonyl)-amino]-butyric acid methyl ester 
• 66325-66-4 1β,2β,3α,5αβ-tetraacetoxycyclohexane 
• 860812-19-7 4-[((3R,5R)-1,3,4,5-Tetraacetoxy-cyclohexanecarbonyl)-amino]-butyric acid methyl ester 

Relevant articles and documents

Novel quercetin derivatives, their preparation, pharmaceutical compositions containing them and their use

The invention relates to novel quercetin derivatives and pharmaceutically acceptable salts, hydrates, and solvates and dimers thereof; a process for the preparation of the novel quercetin derivatives and pharmaceutically acceptable salts, hydrates, and so

THE INVENTION OF NEW RADICAL CHAIN REACTIONS. PART VIII. RADICAL CHEMISTRY OF THIOHYDROXAMIC ESTERS; A NEW METHOD FOR THE GENERATION OF CARBON RADICALS FROM CARBOXYLIC ACIDS.

The aliphatic and alicyclic esters of N-hydroxy-pyridine-2-thione are readily reduced by tributylstannane in a radical chain reaction to furnish nor-alkanes.In the absence of the stannane a smooth decarboxylative rearrangement occurs to give 2-substituted thiopyridines.The radicals present in this reaction provoke with t-butylthiol an efficient radical reaction with formation of nor-alkane and 2-pyridyl-t-butyl disulphide.Similarly these carbon radicals can be captured by halogen atom transfer to give noralkyl chlorides, bromides and iodides.With oxygen in the presence of t-butylthiol the corresponding noralkyl hydroperoxides are formed in another radical chain reaction.