42442-75-1

Basic information

• Product Name: (1R,2R,3R,4S,5R,6R)-2,3,4,6-tetrakis(acetyloxy)-5-methoxycyclohexyl acetate
• Synonyms: (1R,2R,3R,4S,5R,6R)-2,3,4,6-tetrakis(acetyloxy)-5-methoxycyclohexyl acetate
• CAS NO: 42442-75-1
• Molecular Weight: 404.371
• Mol File: 42442-75-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1R,2R,3R,4S,5R,6R)-2,3,4,6-tetrakis(acetyloxy)-5-methoxycyclohexyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,3R,4S,5R,6R)-2,3,4,6-tetrakis(acetyloxy)-5-methoxycyclohexyl acetate(42442-75-1)
• EPA Substance Registry System: (1R,2R,3R,4S,5R,6R)-2,3,4,6-tetrakis(acetyloxy)-5-methoxycyclohexyl acetate(42442-75-1)

Safety Data

• Hazardous Substances Data: 42442-75-1(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 10284-63-6 pinitol 
• 18391-50-9 (1R)-O¹,O⁵,O⁶-triacetyl-O⁴-methyl-2,3-anhydro-allo-inositol 
• 6090-97-7 (1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol 
• 145107-29-5 (+)-Conduritol E epoxide 
• 57090-00-3 2,3-anhydro-allo-inositol 
• 551-72-4 inositol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1158414-58-4 D-1,2,4,5-tetra-O-acetyl-3-O-methyl-chiro-inositol 
• 1158414-54-0 D-1,2,3,5-tetra-O-acetyl-4-O-methyl-chiro-inositol 

Relevant articles and documents

MULTIBIOTIC AGENTS AND METHODS OF USING THE SAME

Multibiotic agents are disclosed. The multibiotic agents may contain two or more moieties linked through bonds cleavable in vivo. The bonds cleavable in vivo can be ester bonds, amide bonds, azo bonds, glycosidic bonds, carbonate linkers, or carbamate linkers. The moieties can be alcohol cores, amine cores, and/or acyls. Also disclosed are compositions containing multibiotic agents and methods of using the multibiotic agents.

Semi-synthetic analogs of pinitol as potential inhibitors of TNF-α cytokine expression in human neutrophils

Semi-synthetic analogs of pinitol were subjected to screening by determining TNF-α expression in human neutrophils using flowcytometry. Among the tested compounds, three derivatives displayed more than 50% inhibition of TNF-α cytokine secretion in LPS ind

The Structure and Stereochemistry of D(+)-Pinitol: Application of 2D-NMR Spectroscopy

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