123808-78-6

Basic information

• Product Name: (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate
• Synonyms: (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate
• CAS NO: 123808-78-6
• Molecular Weight: 315.323
• Mol File: 123808-78-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate(123808-78-6)
• EPA Substance Registry System: (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate(123808-78-6)

Safety Data

• Hazardous Substances Data: 123808-78-6(Hazardous Substances Data)

Upstream product

• 123808-77-5 conduramine A-1 tetraacetate 
• 138430-38-3 (1S,2R,3S,6R)-6-Acetamido-1,2-O-isopropylidenecyclohex-4-ene-1,2,3-triol 
• 123808-75-3 (1S,4R,7S,8S)-(+)-7,8-diacetoxy-2-oxa-3-azabicyclo<2.2.2>oct-5-ene hydrochloride 
• 108-24-7 acetic anhydride 
• 77803-81-7 r-1-Acetamido-t-3-bromcyclohexan-c-2,c-4-diyldiacetat 
• 77803-77-1 (1S*,4R*)-4-aminocyclohex-2-enol 
• 56239-25-9 (+/-)-2-Oxa-3-azabicyclo[2.2.2]oct-5-ene hydrochloride 
• 77803-78-2 cis-1-Acetamido-2-cyclohexen-4-ylacetat 
• 77803-85-1 r-1-Acetamido-c-2,c-3-epoxy-c-4-cyclohexylacetat 
• 86504-11-2 cis-3,5-cyclohexadiene-1,2-diol diacetate 
• 17793-95-2 cis-1,2-dihydrocatechol 
• 138448-93-8 3-Acetyl-1-bromo-5,6-O-isopropylidene-2-oxa-3-azabicyclo<2.2.2>oct-7-ene-5,6-diol 
• 92501-72-9 N-((1R,2S,3R,4S)-2,3,4-Trihydroxy-cyclohexyl)-acetamide 
• 67451-62-1 cis-(1S,2S)-1,2-dihydroxy-3-bromocyclohexa-3,5-diene 

Relevant articles and documents

Stereospecific synthesis of aminocyclitols via cycloadditions of unsymmetrical, optically pure dienes: Conduramine A-1 and Dihydroconduramine A-1

Stereospecific synthesis of Conduramine A-1 and Dihydroconduramine A-1 has been achieved by a fully regio- and stereospecific hetero Diels-Alder cycloaddition of a nitrosyl derivative and homochiral 1-halocyclohexadiene diols obtained by microbial oxidati

Asymmetric Synthesis of cis-1,3-Diamino-1,3-dideoxycyclitols

Starting with the hetero-Diels-Alder reaction of the O-isopropylidene-protected cis-cyclohexa-3,5-diene-1,2-diol with (-)-2,3:5,6-di-O-isopropylidene-1-nitroso-α-D-manno-furanosyl chloride the optically pure (+)-endo-adduct was exclusively formed.After re

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, IV. - Preparation and Stereochemistry of Dideoxyinosamine Derivatives

The general method for the synthesis of polyhydroxy amines by Diels-Alder reactions with a nitroso compound, reduction of the adduct with cleavage of the N - O bond and hydroxylation of the remaining C = C -double bond, can also be realized with α-chloronitrosocyclohexane as dienophile, in good yield.Primary amines are synthesized in this way.