5263-58-1

Basic information

• Product Name: Benzeneethanamine, N-2-propenyl-
• CAS NO: 5263-58-1
• Molecular Formula: C11H15N
• Molecular Weight: 161.247
• Mol File: 5263-58-1.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzeneethanamine, N-2-propenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanamine, N-2-propenyl-(5263-58-1)
• EPA Substance Registry System: Benzeneethanamine, N-2-propenyl-(5263-58-1)

Safety Data

• Hazardous Substances Data: 5263-58-1(Hazardous Substances Data)

Upstream product

• 4383-22-6 Allylbenzylamine 
• 23696-40-4 trimethylstannylmethyl iodide 
• 103-63-9 1-phenyl-2-bromoethane 
• 107-11-9 1-amino-2-propene 
• 6125-24-2 2-Phenylnitroethane 
• 591-87-7 Allyl acetate 
• 64-04-0 phenethylamine 
• 106-95-6 allyl bromide 
• 6728-21-8 allyl mesylate 
• 105824-25-7 C₁₁H₁₃N 
• 70867-37-7 1-(allyloxycarbonyl)phenethylamine 
• 74974-19-9 benzylmethyleneimine 
• 10017-11-5 allylammonium chloride 

Downstream Products

• 116741-71-0 N-phenylethyl allylamino-2 ethanethiol-1 
• 10135-23-6 N-(2-phenylethyl)pyrrolidin-2-one 
• 87463-22-7 N-Allyl-N-(2-phenylethyl)-3(E),5-hexadienamide 
• 64-04-0 phenethylamine 
• 1276126-38-5 C₁₈H₂₃NO₃ 
• 1276126-48-7 C₁₆H₁₉NO₃ 
• 798542-77-5 N-hydroxy-3-(2-oxo-1-phenethyl-2,5-dihydro-1H-pyrrol-3-yl)-propionamide 

Relevant articles and documents

Direct Reductive N-Functionalization of Aliphatic Nitro Compounds

The first general protocol for the direct reductive N-functionalization of aliphatic nitro compounds is presented. The nitro group is partially reduced to a nitrenoid, with a mild and readily available combination of B2pin2 and zinc organyls. Thereby, the formation of an unstable nitroso intermediate is avoided, which has so far severely limited reductive transformations of aliphatic nitro compounds. The reaction is concluded by an electrophilic amination of zinc organyls.

PRODUCTION METHOD FOR 2-ALKENYLAMINE COMPOUND

Provided is a method for producing a 2-alkenylamine compound efficiently and at low cost, using a primary or secondary amine compound and a 2-alkenyl compound as the starting materials therefor. The 2-alkenyleamine compound is produced by 2-alkenylating a primary or secondary amine compound, using a specified 2-alkenylating agent and in the presence of a catalyst comprising a complexing agent and a transition metal precursor stabilized by a monovalent anionic five-membered conjugated diene.

PRODUCTION METHOD FOR 2-ALKENYLAMINE COMPOUND

Provided is a method for producing a 2-alkenylamine compound efficiently and at low cost, using a primary or secondary amine compound and a 2-alkenyl compound as the starting materials therefor. The 2-alkenylamine compound is produced by adding Bronsted acid when 2-alkenylating by reacting the primary or secondary amine compound with the 2-alkenyl compound, and 2-alkenylating in the presence of a catalyst comprising a complexing agent and a transition metal precursor stabilized by a monovalent anionic five-membered conjugated diene.