22057-80-3

Basic information

• Product Name: N,N-dimethyl-4-(1-phenylethenyl)aniline
• CAS NO: 22057-80-3
• Molecular Formula: C₁₆H₁₇N
• Molecular Weight: 223.3129
• Mol File: 22057-80-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 353.1°C at 760 mmHg
• Flash Point: 143.5°C
• Density: 1.015g/cm³
• Vapor Pressure: 3.66E-05mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: N,N-dimethyl-4-(1-phenylethenyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-4-(1-phenylethenyl)aniline(22057-80-3)
• EPA Substance Registry System: N,N-dimethyl-4-(1-phenylethenyl)aniline(22057-80-3)

Safety Data

• Hazardous Substances Data: 22057-80-3(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 530-44-9 4-(Dimethylamino)benzophenone 
• 23308-55-6 1,1-bis-(4-dimethylamino-phenyl)-1-phenyl-ethane 
• 768295-58-5 1-[4-(dimethylamino)phenyl]-1-phenylethanol 
• 121-69-7 N,N-dimethyl-aniline 
• 98-86-2 acetophenone 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 
• 98-81-7 1-bromovinylbenzene 
• 28611-39-4 4-(dimethylamino)benzene-boronic acid 
• 68587-15-5 (4-(dimethylamino)phenyl)(p-tolyl)methanone 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 63269-86-3 3-methyl-3-phenyl-3H-diazirine 
• 621-82-9 Cinnamic acid 

Downstream Products

• 55252-43-2 N,N-dimethyl-4-[(E)-(4-nitrophenyl)diazenyl]aniline 
• 1081768-03-7 4'-Chloro-4-dimethylaminoazobenzene 

Relevant articles and documents

The Concept of Photozymes: Short Peptides with Photoredox Catalytic Activity for Nucleophilic Additions to α-Phenyl Styrenes

Conventional photoredox catalytic additions of alcohols to olefins require additives, like thiophenol, to promote back electron transfer. The concept of “photozymes” assumes that forward and backward electron transfer steps in a photoredox catalytic cycle

Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditions

Nickel-catalyzed addition of arylboron reagents to ketones results in aryl olefins directly. The neutral condition allows acidic protons of alcohols, phenols, and malonates to be present, and fragile structures are also tolerated.

Microwave-assisted, Pd(0)-catalyzed cross-coupling of diazirines with aryl halides

Pd(0)-catalyzed cross-coupling reactions of diazirines with aryl halides under microwave heating conditions afford a series of substituted olefins. A reaction mechanism involving the migratory insertion of the Pd carbene intermediate is proposed.