65001-46-9

Basic information

• Product Name: Benzenamine, 3,5-dimethyl-2-(2-propenyl)-
• CAS NO: 65001-46-9
• Molecular Formula: C11H15N
• Molecular Weight: 161.247
• Mol File: 65001-46-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3,5-dimethyl-2-(2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3,5-dimethyl-2-(2-propenyl)-(65001-46-9)
• EPA Substance Registry System: Benzenamine, 3,5-dimethyl-2-(2-propenyl)-(65001-46-9)

Safety Data

• Hazardous Substances Data: 65001-46-9(Hazardous Substances Data)

Upstream product

• 203321-89-5 (3,5-dimethylphenyl)carbamic acid 1,1-dimethylethyl ester 
• 108-69-0 3,5-dimethylaminoaniline 
• 65001-45-8 N-allyl-3,5-dimethylbenzenamine 
• 51625-18-4 N-Allyl-N-benzoyl-3,5-dimethyl-anilin 
• 25050-22-0 N-(3,5-dimethylphenyl)-benzamide 

Downstream Products

• 65001-48-1 (Z)-3,5-Dimethyl-2-(1'-propenyl)-anilin 
• 65001-49-2 (E)-3,5-Dimethyl-2-(1'-propenyl)-anilin 
• 882788-18-3 N-(2-allyl-3,5-dimethyl-phenyl)-3-(3-chloro-phenyl)-acrylamide 
• 1424370-24-0 2-allyl-3,5-dimethyl-N-(3-methylbut-2-enyl)aniline 
• 1424370-33-1 2-allyl-N-(trans-cinnamyl)-3,5-dimethylaniline 

Relevant articles and documents

Copper-catalyzed radical cascade cyclization for the synthesis of phosphorated indolines

A novel and convenient approach to the synthesis of various phosphorated indolines via a copper-catalyzed radical cascade cyclization reaction has been developed. The reaction employs cheap copper as the catalyst and K2S2O8 as the oxidant under mild conditions. Various alkenes and P-radical precursors are compatible with this transformation. Preliminary mechanistic studies reveal that the addition of the P-radical may initiate the reaction, and then oxidative cyclization may be achieved to afford the desired product. This journal is

Stereoselective synthesis of novel 2-alkenyl-2,3,4,5-tetrahydro-1,4-epoxy- 1-benzazepines and 2-alkenyl-2,3,4,5-tetrahydro-1H-1-benzazepin-4-ols

New series of polyfunctionalized 2,3,4,5-tetrahydro-1,4-epoxy-1- benzazepines and 2,3,4,5-tetrahydro-1H-1-benzazepin-4-ols substituted at C2 with 2-methylprop-1-enyl, (E)-styryl, and (E)-pent-1-enyl were synthesized starting from the corresponding N-alken

Pd(II)-catalyzed enantioselective oxidative tandem cyclization reactions. Synthesis of indolines through C-N and C-C bond formation

We have developed an efficient Pd(II)-catalyzed enantioselective oxidative tandem cyclization strategy using molecular oxygen as a green oxidant for the double 5-exo-trig cyclizations of N-(2-allylaryl) amides to afford a variety of indolines in good yiel