26344-04-7

Basic information

• Product Name: (1R,2R)-2-(2,4-dinitrophenylamino)cyclohexanol
• Synonyms: (1R,2R)-2-(2,4-dinitrophenylamino)cyclohexanol
• CAS NO: 26344-04-7
• Molecular Weight: 281.268
• Mol File: 26344-04-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,2R)-2-(2,4-dinitrophenylamino)cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-2-(2,4-dinitrophenylamino)cyclohexanol(26344-04-7)
• EPA Substance Registry System: (1R,2R)-2-(2,4-dinitrophenylamino)cyclohexanol(26344-04-7)

Safety Data

• Hazardous Substances Data: 26344-04-7(Hazardous Substances Data)

Upstream product

• 189942-49-2 (4R,5R)-trans-hexahydrobenzoxazolidin-2-one 
• 286-20-4 cyclohexane-1,2-epoxide 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 13374-31-7 (1R,2R)-trans-2-aminocyclohexanol hydrochloride 
• 931-15-7 (1R,2R)-2-aminocyclohexanol 
• 155975-19-2 (1R,2R)-trans-2-(N-tert-butyloxycarbonyl)amino-1-cyclohexanol 
• 96788-81-7 (1R,2R)-2-Aminocyclohexanol (+)tartrate 

Downstream Products

• 96027-56-4 (1R,2R)-2-(2,4-Dinitroanilino)cyclohexyl Benzoate 

Relevant articles and documents

A practical method for the synthesis of highly enantioenriched trans -1,2-amino alcohols

A highly enantioselective addition of phenyl carbamate to meso-epoxides has been developed to efficiently generate protected trans-1,2-amino alcohols. This transformation is promoted by an oligomeric (salen)Co-OTf catalyst and has been used to prepare two useful 2-aminocycloalkanol hydrochlorides in enantiopure form on a multigram scale from commercially available starting materials.

A Method for Determinig Absolute Configuration of Cycloalkanamines and Related Compounds by CD Spectra of Their 2,4-Dinitrophenyl Derivatives

N-(2,4-Dinitrophenyl) derivatives of cycloalkanamines and related compounds having an amino and an aromatic groups in vicinal positions were prepared.Their CD spectra exhibited marked Cotton effect around 400nm, the sign of which was shown to coincide wit