127598-83-8

Basic information

• Product Name: Benzenamine, 4-methyl-N-[(2E)-3-phenyl-2-propenyl]-
• CAS NO: 127598-83-8
• Molecular Formula: C16H17N
• Molecular Weight: 223.318
• Mol File: 127598-83-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methyl-N-[(2E)-3-phenyl-2-propenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methyl-N-[(2E)-3-phenyl-2-propenyl]-(127598-83-8)
• EPA Substance Registry System: Benzenamine, 4-methyl-N-[(2E)-3-phenyl-2-propenyl]-(127598-83-8)

Safety Data

• Hazardous Substances Data: 127598-83-8(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 118714-21-9 4-phenyl-1-p-tolyl-1-azabuta-1,3-diene 
• 15286-48-3 (E)-4-methyl-N-((E)-3-phenylallylidene)aniline 
• 14371-10-9 (E)-3-phenylpropenal 
• 106625-69-8 ethyl (E)-3-phenyl-2-propenyl carbonate 
• 118714-24-2 N-cinnamylidene-p-toluidine hydrochloride 

Downstream Products

• 127598-84-9 N-cinnamyl N-(2-cyanoethyl)-4-methylaniline 
• 1421518-02-6 N-(4-methylphenyl)-N-[(2E)-3-phenylprop-2-en-1-yl]urea 
• 76061-97-7 4-Phenyl-6-methylquinoline 
• 76061-95-5 4-Phenyl-6-methyl-1,2,3,4-tetrahydroquinoline 
• 104-55-2 3-phenyl-propenal 
• 118072-35-8 3-(2-Dimethylaminomethyl-4-methyl-phenylamino)-propionitrile 

Relevant articles and documents

First example of the cascade acylation/IMDAV/ene reaction sequence, leading to N-arylbenzo[f]isoindole-4-carboxylic acids possessing anti-viral activity

The reaction between readily accessible N-aryl-3-phenylallylamines and maleic anhydride led to unexpected products – polysubstituted hydrogenated benzo[f]isoindole-4-carboxylic acids. This transformation proceeds through a previously unknown sequence of s

Air Stable Iron(II) PNP Pincer Complexes as Efficient Catalysts for the Selective Alkylation of Amines with Alcohols

A series of well-defined iron(II) complexes of the types [Fe(PNP)Br2] and [Fe(PNP)(CO)Br2] with PNP pincer ligands based on triazine and pyridine backbones were prepared and fully characterized. These complexes were tested as catalysts for the alkylation of amines by alcohols. The high-spin complexes [Fe(PNP)Br2] are catalytically inactive. The low-spin complexes [Fe(PNP)(CO)Br2] bearing a carbonyl co-ligand efficiently and selectively convert primary alcohols and aromatic and benzylic amines selectively into mono-N-alkylated amines in good to excellent isolated yields. A mechanistic proposal is given. (Figure presented.).

Solvent-free synthesis, DNA-topoisomerase II activity and molecular docking study of new asymmetrically N,N′-substituted ureas

A new series of asymmetrically N,N′-substituted ureas 20-25 was prepared using solvent free conditions, which is an eco-friendly methodology, starting with Schiff bases derived from cinnamaldehyde and p-substituted anilines, which are subsequently submitt