127660-90-6

Basic information

• Product Name: N-(Cycloheptylmethyl)-N-phenylamine
• Synonyms: N-(Cycloheptylmethyl)-N-phenylamine
• CAS NO: 127660-90-6
• Molecular Weight: 203.327
• Mol File: 127660-90-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N-(Cycloheptylmethyl)-N-phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Cycloheptylmethyl)-N-phenylamine(127660-90-6)
• EPA Substance Registry System: N-(Cycloheptylmethyl)-N-phenylamine(127660-90-6)

Safety Data

• Hazardous Substances Data: 127660-90-6(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 100-62-9 N-methylenebenzenamine 
• 291-64-5 cycloheptane 
• 100-61-8 N-methylaniline 
• 628-92-2 Cycloheptene 
• 191664-06-9 4-Chloro-benzenesulfonic acid cycloheptylmethyl ester 
• 191664-05-8 Benzenesulfonic acid cycloheptylmethyl ester 
• 17595-82-3 cycloheptylmethyl p-nitrobenzenesulfonate 
• 16472-98-3 cycloheptylmethyl 4-methylbenzenesulfonate 
• 638-54-0 1,8-octanedial 

Relevant articles and documents

Selective synthesis of N-(cyclohexylmethyl)-N-alkylamines from primary amines and pimelaldehyde using tetracarbonylhydridoferrate, HFe(CO)4-, as a reducing reagent

Treatment of primary amines with pimelaldehyde in the presence of tetracarbonyl-hydridoferrate, HFe(CO)4- at room temperature under atmospheric pressure of CO for 24 hours gave selectively corresponding N-(cyclohexylmethyl)-N-alkylam

GROUP 5 METAL COMPLEXES FOR PRODUCING AMINE-FUNTIONALIZED POLYOLEFINS

This application pertains to group 5 metal complexes having the structure of Formula I: and their potential utility in catalyzing amination of polyolefins having alkene groups.amine-

Catalytic and Atom-Economic Csp3 ?Csp3 Bond Formation: Alkyl Tantalum Ureates for Hydroaminoalkylation

Atom-economic and regioselective Csp3 ?Csp3 bond formation has been achieved by rapid C?H alkylation of unprotected secondary arylamines with unactivated alkenes. The combination of Ta(CH2SiMe3)3Clsu