86992-79-2

Basic information

• Product Name: 3,5-Cyclohexadiene-1,2-diol, 3-chloro-, (1R,2R)-rel-
• CAS NO: 86992-79-2
• Molecular Formula: C6H7ClO2
• Molecular Weight: 146.573
• Mol File: 86992-79-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 3,5-Cyclohexadiene-1,2-diol, 3-chloro-, (1R,2R)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Cyclohexadiene-1,2-diol, 3-chloro-, (1R,2R)-rel-(86992-79-2)
• EPA Substance Registry System: 3,5-Cyclohexadiene-1,2-diol, 3-chloro-, (1R,2R)-rel-(86992-79-2)

Safety Data

• Hazardous Substances Data: 86992-79-2(Hazardous Substances Data)

Upstream product

• 108-90-7 chlorobenzene 

Downstream Products

• 140706-53-2 (1R,2S,3S,4S)-5-Chloro-cyclohex-5-ene-1,2,3,4-tetraol 
• 176166-15-7 cis-(1S,2S)-1,2-dihydroxy-3-chlorocyclohex-3-ene 
• 951327-35-8 C₁₄H₁₅ClO₅ 
• 1190605-22-1 C₆H₈BrClO₃ 
• 108-43-0 3-monochlorophenol 
• 95-57-8 2-monochlorophenol 
• 1392229-39-8 (4S,5S)-4,5-bis((tert-butyldimethylsilyl)oxy)-3-chlorocyclohex-2-en-1-one 
• 1392229-29-6 (4S,5S)-3-chloro-4,5-dihydroxycyclohex-2-enone 
• 1042952-07-7 C₁₄H₁₃ClO₃ 
• 138430-37-2 (1S,2R,3S,6R)-6-Benzyloxycarbonylamino-1,2-O-isopropylidenecyclohex-4-ene-1,2,3-triol 
• 138448-91-6 3-(benzyloxycarbonyl)-1-chloro-5,6-O-isopropylidene-2-oxa-3-azabicyclo<2.2.2>oct-7-ene-5,6-diol 
• 138430-39-4 ((3aS,4R,7aS)-2,2-Dimethyl-7-oxo-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-4-yl)-carbamic acid benzyl ester 
• 138513-22-1 dihydroconduramine A-1 
• 137567-79-4 (1R,2R,3R,4R)-5-cyclohexene-1,2,3,4-tetrol 

Relevant articles and documents

Concise chemoenzymatic synthesis of methyl d-2,3-dideoxyriboside

The synthesis of methyl α- and β-d-2,3-dideoxyriboside from a non-carbohydrate source is presented. The source of chirality is the microbial oxidation of halobenzenes to produce cyclohexadienediols, which are transformed into the final product in five steps with high chemical and enantiomeric purity.

1-chloro-(2S,3S)-dihydroxycyclohexa-4,6-diene [ 3,5-Cyclohexadiene-1,2-diol, 3-chloro-, (1S-cis)- ]

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Enantioselective Bacterial Biotransformation Routes to cis-Diol Metabolites of Monosubstituted Benzenes, Naphthalene and Benzocycloalkenes of Either Absolute Configuration

Enzyme-catalysed kinetic resolution and asymmetric dihydroxylation routes to enantiopure cis-diol metabolites of arenes and benzocycloalkenes of either absolute configuration have been developed using appropriate strains of the bacterium Pseudomonas putida.