1258204-09-9

Basic information

• Product Name: (1R,2R)-N¹,N¹-dipentylcyclohexane-1,2-diamine
• Synonyms: (1R,2R)-N¹,N¹-dipentylcyclohexane-1,2-diamine
• CAS NO: 1258204-09-9
• Molecular Weight: 254.459
• Mol File: 1258204-09-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R)-N¹,N¹-dipentylcyclohexane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-N¹,N¹-dipentylcyclohexane-1,2-diamine(1258204-09-9)
• EPA Substance Registry System: (1R,2R)-N¹,N¹-dipentylcyclohexane-1,2-diamine(1258204-09-9)

Safety Data

• Hazardous Substances Data: 1258204-09-9(Hazardous Substances Data)

Downstream Products

• 1411983-37-3 3-(((1R,2R)-2-(dipentylamino)cyclohexyl)amino)-4-((4-(trifluoromethyl)benzyl)amino)cyclobut-3-ene-1,2-dione 
• 1411983-38-4 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1R,2R)-2-(dipentylamino)cyclohexyl)amino)cyclobut-3-ene-1,2-dione 
• 1411983-39-5 3-(((1R,2R)-2-(dipentylamino)cyclohexyl)amino)-4-((4-(trifluoromethyl)phenyl)amino)cyclobut-3-ene-1,2-dione 
• 1411983-40-8 3-((3,5-bis(trifluoromethyl)phenyl)amino)-4-(((1R,2R)-2-(dipentylamino)cyclohexyl)amino)cyclobut-3-ene-1,2-dione 

Relevant articles and documents

Tertiary aminourea-catalyzed enantioselective iodolactonization

Binding the anion : A highly enantioselective iodolactonization of 5-hexenoic acids has been achieved using a tertiary aminourea-catalyst (see scheme). The use of catalytic iodine in this process is critical to enhancing both the reactivity and enantioselectivity of the stoichiometric I+ source. The mechanism is proposed to involve binding of an iodonium imidate intermediate by the H-bond donor catalyst.