65001-45-8

Basic information

• Product Name: N-allyl-3,5-dimethylbenzenamine
• Synonyms: N-allyl-3,5-dimethylbenzenamine
• CAS NO: 65001-45-8
• Molecular Weight: 161.247
• Mol File: 65001-45-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-allyl-3,5-dimethylbenzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-allyl-3,5-dimethylbenzenamine(65001-45-8)
• EPA Substance Registry System: N-allyl-3,5-dimethylbenzenamine(65001-45-8)

Safety Data

• Hazardous Substances Data: 65001-45-8(Hazardous Substances Data)

Upstream product

• 108-69-0 3,5-dimethylaminoaniline 
• 107-18-6 allyl alcohol 
• 203321-89-5 (3,5-dimethylphenyl)carbamic acid 1,1-dimethylethyl ester 
• 22445-41-6 3,5-dimethylphenyl iodide 
• 107-11-9 1-amino-2-propene 
• 25050-22-0 N-(3,5-dimethylphenyl)-benzamide 
• 106-95-6 allyl bromide 
• 51625-18-4 N-Allyl-N-benzoyl-3,5-dimethyl-anilin 

Downstream Products

• 65001-46-9 2-allyl-3,5-dimethylaniline 
• 1380209-21-1 2-allyl-1-azido-3,5-dimethylbenzene 
• 1251443-42-1 N-(2-allyl-3,5-dimethyl-phenyl)-4-methylbenzenesulfonamide 
• 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 
• 65001-49-2 (E)-3,5-Dimethyl-2-(1'-propenyl)-anilin 
• 65001-48-1 (Z)-3,5-Dimethyl-2-(1'-propenyl)-anilin 

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

Ligands for copper-catalyzed C-N bond forming reactions with 1 Mol% CuBr as catalyst

Several new ligands were designed to promote copper-catalyzed Ullman C-N coupling reactions. In this group, 8-hydroxyquinolin-N-oxide was found to serve as a superior ligand for CuBr-catalyzed coupling reactions of aryl iodides, bromides, and chlorides with aliphatic amines and N-heterocycles under a low catalyst loading (1% [Cu] mol). Reactions with the inexpensive catalytic system display a high functional group tolerance as well as excellent chemoselectivity.

Novel strategies for the solid phase synthesis of substituted indolines and indoles

Using a polymer-bound selenenyl bromide resin, o-allyl and o-prenyl anilines were cycloaded to afford a series of solid-supported indoline and indole scaffolds. These scaffolds were then functionalized and cleaved via four distinct methods, namely traceless reduction, radical cyclization, radical rearrangement, and oxidative elimination, to afford 2-methyl indolines, polycyclic indolines, 2-methyl indoles, and 2-propenyl indolines, respectively. A number of small combinatorial libraries of compounds reminiscent of certain designed ligands of biological interest were constructed demonstrating the potential utility of the developed methodology to chemical biology studies and the drug discovery process.