1384282-27-2

Basic information

• Product Name: (1S,2S,4S,5S)-N₂,N₅-dibenzyl-N₂,N₅-dimethylbicyclo[2.2.1]heptane-2,5-diamine
• Synonyms: (1S,2S,4S,5S)-N₂,N₅-dibenzyl-N₂,N₅-dimethylbicyclo[2.2.1]heptane-2,5-diamine
• CAS NO: 1384282-27-2
• Molecular Weight: 334.505
• Mol File: 1384282-27-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,4S,5S)-N₂,N₅-dibenzyl-N₂,N₅-dimethylbicyclo[2.2.1]heptane-2,5-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,4S,5S)-N₂,N₅-dibenzyl-N₂,N₅-dimethylbicyclo[2.2.1]heptane-2,5-diamine(1384282-27-2)
• EPA Substance Registry System: (1S,2S,4S,5S)-N₂,N₅-dibenzyl-N₂,N₅-dimethylbicyclo[2.2.1]heptane-2,5-diamine(1384282-27-2)

Safety Data

• Hazardous Substances Data: 1384282-27-2(Hazardous Substances Data)

Upstream product

• 103-67-3 benzyl-methyl-amine 
• 145092-68-8 (S,S)-bicyclo<2.2.1>heptane-2,5-dione 
• 5888-36-8 (1S,2R,4S,5R)-2,5-dihydroxybicyclo[2.2.1]heptane 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 50-00-0 formaldehyd 
• 698353-48-9 C₂₁H₂₆N₂ 

Relevant articles and documents

Evaluation of the chiral DIANANE backbone as ligand for organolithium reagents

Novel endo,endo-2,5-diaminonorbonane-derived tertiary C2- symmetrical diamines were synthesized via the one-pot reductive amination of enantiomerically pure norbornane-2,5-dione. These ligands were applied to various catalytic reactions such as asymmetric deprotonation, asymmetric bromine-lithium exchange, and enantioselective addition of aryl- and allkylithium reagents to aromatic aldimines. Copyright