320410-59-1

Basic information

• Product Name: (1S,2S,3S,4S)-5-iodo-5-cyclohexene-1,2,3,4-tetraol
• Synonyms: (1S,2S,3S,4S)-5-iodo-5-cyclohexene-1,2,3,4-tetraol
• CAS NO: 320410-59-1
• Molecular Weight: 272.04
• Mol File: 320410-59-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S,2S,3S,4S)-5-iodo-5-cyclohexene-1,2,3,4-tetraol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3S,4S)-5-iodo-5-cyclohexene-1,2,3,4-tetraol(320410-59-1)
• EPA Substance Registry System: (1S,2S,3S,4S)-5-iodo-5-cyclohexene-1,2,3,4-tetraol(320410-59-1)

Safety Data

• Hazardous Substances Data: 320410-59-1(Hazardous Substances Data)

Upstream product

• 138769-92-3 cis-(1S,2S)-1,2-dihydroxy-3-iodocyclohexa-3,5-diene 

Downstream Products

• 320410-63-7 (1S,2R,5R,6R)-6-(acetyloxy)-2,5-dibromo-3-iodo-3-cyclohexenyl acetate 

Relevant articles and documents

Chemoenzymatic synthesis of carbasugars (+)-pericosines A-C from diverse aromatic cis-dihydrodiol precursors

cis-Dihydrocatechols, derived from biological cis-dihydroxylation of methyl benzoate, iodobenzene and benzonitrile, using the microorganism Pseudomonas putida UV4, were converted into pericosines A, C, and B, respectively. This approach constitutes the shortest syntheses, to date, of these important natural products with densely packed functionalities.

Enantiopure arene dioxides: Chemoenzymatic synthesis and application in the production of trans-3,4-dihydrodiols

Enantiopure syn- and anti-arene dioxides are synthesised from cis-dihydrodiol metabolites; anti-benzene dioxides are reduced to enantiopure trans-3,4-dihydrodiols while synbenzene dioxides racemise thermally via 1,4-dioxocins.