156257-14-6

Basic information

• Product Name: Acetamide, N,N'-(1R,2R)-1,2-cyclohexanediylbis-
• Synonyms: (1R,2R)-trans-1,2-diacetamidocyclohexane;trans-1,2-Diacetamido-cyclohexan;(R,R)-N,N'-diacetyl-1,2-diaminocyclohexane;catena-(R,R)-1,2-diacetamidocyclohexane;N-((1R,2R)-2-Acetylamino-cyclohexyl)-acetamide
• CAS NO: 156257-14-6
• Molecular Formula: C10H18N2O2
• Molecular Weight: 198.265
• Mol File: 156257-14-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Acetamide, N,N'-(1R,2R)-1,2-cyclohexanediylbis-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N,N'-(1R,2R)-1,2-cyclohexanediylbis-(156257-14-6)
• EPA Substance Registry System: Acetamide, N,N'-(1R,2R)-1,2-cyclohexanediylbis-(156257-14-6)

Safety Data

• Hazardous Substances Data: 156257-14-6(Hazardous Substances Data)

Upstream product

• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 32044-22-7 (1R,2R)-1,2-diaminocyclohexane tartrate 

Downstream Products

• 220665-65-6 (1R,2R)-N₁,N₂-diethylcyclohexane-1,2-diamine 

Relevant articles and documents

Synthesis, crystal structure, IR and Raman properties of 1,2-diacetamidocyclohexane and its complexes with ZnBr2 and HBr 3

X-ray crystallography, infrared absorption and Raman scattering were applied to study the influence of Zn(II) or H+ on the amidic bond. (R,R)-1,2-diacetamidocyclohexane (DAACH) was chosen as a conformationally strained chiral building block inc

Supramolecular-directed chiral induction in biaryl derivatives

(Chemical Equation Presented) A thermodynamically controlled resolution has allowed for the generation of diastereomerically enriched complexes, by chirality transfer from an enantiopure building block to a dynamically racemic biaryl derivative. A switcha

N,N'-dialkylated 1,2-diamine derivatives as new efficient ligands for RuCl2(PPh3)3 catalyzed asymmetric transfer hydrogenation of aromatic ketones

Chiral N,N'-dialkylated cyclohexanediamine derivatives ligands have been synthesized and used in an asymmetric transfer hydrogenation of aryl ketones. Optically active alcohols with up to 93% enantiomeric excess were obtained in high yield.