860994-91-8

Basic information

• Product Name: 1,2-Cyclohexanediamine, N,N-dipropyl-, (1R,2R)-
• CAS NO: 860994-91-8
• Molecular Formula: C12H26N2
• Molecular Weight: 198.352
• Mol File: 860994-91-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Cyclohexanediamine, N,N-dipropyl-, (1R,2R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclohexanediamine, N,N-dipropyl-, (1R,2R)-(860994-91-8)
• EPA Substance Registry System: 1,2-Cyclohexanediamine, N,N-dipropyl-, (1R,2R)-(860994-91-8)

Safety Data

• Hazardous Substances Data: 860994-91-8(Hazardous Substances Data)

Upstream product

• 1197208-38-0 N-((1R,2R)-2-aminocyclohexyl)benzamide 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 1379686-02-8 N-[(1R,2R)-2-(dipropylamino)cyclohexyl]benzamide 
• 320778-89-0 N-((1R,2R)-2-aminocyclohexyl)acetamide 

Downstream Products

• 1209485-59-5 (1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate 
• 1209485-61-9 (1R,2R)-2-(dipropylamino)cyclohexanaminium 2,2,2-trifluoroacetate 
• 1379685-92-3 2-[(1R,2R)-2-(dipropylamino)cyclohexylamino]-5,7-bis(trifluoromethyl)quinazolin-4(3H)-one 
• 1379685-88-7 2-[(1R,2R)-2-(dipropylamino)cyclohexylamino]-7-(trifluoromethyl)quinazolin-4(3H)-one 
• 1003922-10-8 (1R,2R)-2-isothiocyanato-N,N-dipropylcyclohexanamine 
• 1003922-03-9 (S)-2-(3-((1R,2R)-2-(dipropylamino)cyclohexyl)thioureido)-N-isopropyl-3,3-dimethylbutanamide 
• 1003922-04-0 (S)-N-((R)-1-(dimethylamino)-3-methyl-1-oxobutan-2-yl)-2-(3-((1R,2R)-2-(dipropylamino)cyclohexyl)thioureido)-3,3-dimethylbutanamide 

Relevant articles and documents

Design and development of bioinspired guanine-based organic catalyst for asymmetric catalysis

Design, preparation, and studies of a family of new organic catalysts are presented. The design of the catalysts is inspired by the ability of DNA nucleobases to develop precise and explicit hydrogen bonds. We have shown that this phenomenon can be used to create a useful organic catalyst that demonstrates a recognition pattern similar to those of common organic substrates. A selected bifunctional catalyst based on a guanine structure has been shown to catalyze the conjugate addition of 1,3-dicarbonyl compounds to various nitroalkenes, providing the products in good yields and enantioselectivities.

Thiourea-catalyzed enantioselective cyanosilylation of ketones

The new chiral amino thiourea catalyst 3d promotes the highly enantioselective cyanosilylation of a wide variety of ketones. The hindered tertiary amine substituent plays a crucial role with regard to both stereoinduction and reactivity, suggesting a coop