80582-74-7

Basic information

• Product Name: (1S,2S,3S,4S)-anti-benzene dioxide
• Synonyms: (1S,2S,3S,4S)-anti-benzene dioxide
• CAS NO: 80582-74-7
• Molecular Weight: 110.112
• Mol File: 80582-74-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (1S,2S,3S,4S)-anti-benzene dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3S,4S)-anti-benzene dioxide(80582-74-7)
• EPA Substance Registry System: (1S,2S,3S,4S)-anti-benzene dioxide(80582-74-7)

Safety Data

• Hazardous Substances Data: 80582-74-7(Hazardous Substances Data)

Upstream product

• 170210-89-6 (+)-(1S,2R,3R,4S)-1,4-diacetoxy-2,3-dibromocyclohex-5-ene 
• 80582-73-6 (1S,2R,3S,6S)-2-bromo-7-oxabicyclo[4.1.0]hept-4-en-3-ol 
• 112212-81-4 (+/-)-(1S,2R,3R,4S)-1,4-diacetoxy-2,3-dibromocyclohex-5-ene 
• 106-51-4 p-benzoquinone 
• 5273-61-0 (5RS,6RS)-5,6-dibromocyclohex-2-ene-1,4-dione 
• 69945-44-4 (1RS,2SR,3RS,4RS)-2,3-dibromocyclohex-5-ene-1,4-diol 

Downstream Products

• 120494-26-0 (1RS,2RS,3RS,6RS)-3,6-diethoxycyclohex-4-ene-1,2-diol 
• 222420-78-2 (1R,2S,3S,4R)-1,4-bis-O-(di-O-benzylphospho)conduritol B 
• 17793-95-2 (1RS,2RS)-cyclohexa-3,5-diene-1,2-diol 
• 146294-06-6 (+/-)-(1,3/2,4)-1,4-Di-O-(2-hydroxyethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 146288-32-6 (+/-)-(1,3/2,4)-2,3-Di-O-acetyl-1,4-di-O-(2-hydroxyethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 146294-07-7 (+/-)-(1,3/2,4)-2,3-Di-O-acetyl-1,4-di-O-(2-triphenylmethoxyethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 114488-20-9 myo-Inositol 1,5,6-trisphosphate 
• 28841-60-3 D-myo-inositol 1,4,5,6-tetrakisphosphate 
• 281206-70-0 5,6-di-O-acetyl-1,4-bis-O-(di-O-benzylphospho)-2,3-bis-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 281206-69-7 5,6-di-O-acetyl-1,4-bis-O-(di-O-benzylphospho)-D-myo-inositol 
• 281206-68-6 (1R,2S,3S,4R)-2,3-di-O-acetyl-1,4-bis-O-(di-O-benzylphospho)conduritol B 

Relevant articles and documents

Synthesis of novel mono and bis-indole conduritol derivatives and their α/β-glycosidase inhibitory effects

Here we synthesized four novel indole conduritol derivatives 1-4 for the first time in the literature and probed their biological activities with the α and β-glucosidases. The compounds showed quite effective glucosidase inhibitory action. IC50

A novel chemo-multienzymatic synthesis of bioactive cyclophellitol and epi-cyclophellitol in both enantiopure forms

A new route to synthesize cyclophellitol and epi-cyclophellitol from racemic starting materials in enantiopure forms has been developed. The synthesis involves a multi-enzymatic biotransformation pathway of the novel cyano-cyclitol (1R,4S,5R,6R)/(1S,4R,5S

Enzyme-assisted total synthesis of the optical antipodes D-myo-inositol 3,4,5-trisphosphate and D-myo-inositol 1,5,6-trisphosphate: Aspects of their structure-activity relationship to biologically active inositol phosphates

Unambiguous total syntheses of both optical antipodes of the enantiomeric pair D-myo-inositol 3,4,5-trisphosphate (Ins(3,4,5)P3) and D- myo-inositol 1,5,6-trisphosphate (Ins(1,5,6)P3) are described. The ring system characteristic of