20021-57-2

Basic information

• Product Name: r-1-Acetamidocyclohexan-t-2,t-3,c-4-triyltriacetat
• CAS NO: 20021-57-2
• Molecular Weight: 315.323
• Mol File: 20021-57-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: r-1-Acetamidocyclohexan-t-2,t-3,c-4-triyltriacetat(CAS DataBase Reference)
• NIST Chemistry Reference: r-1-Acetamidocyclohexan-t-2,t-3,c-4-triyltriacetat(20021-57-2)
• EPA Substance Registry System: r-1-Acetamidocyclohexan-t-2,t-3,c-4-triyltriacetat(20021-57-2)

Safety Data

• Hazardous Substances Data: 20021-57-2(Hazardous Substances Data)

Upstream product

• 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 
• 77803-85-1 r-1-Acetamido-c-2,c-3-epoxy-c-4-cyclohexylacetat 
• 77803-78-2 cis-1-Acetamido-2-cyclohexen-4-ylacetat 

Relevant articles and documents

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.