65178-51-0

Basic information

• Product Name: ALLYL-DIPHENYL-AMINE
• Synonyms: ALLYL-DIPHENYL-AMINE
• CAS NO: 65178-51-0
• Molecular Formula: C₁₅H₁₅N
• Molecular Weight: 209.2863
• Mol File: 65178-51-0.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ALLYL-DIPHENYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL-DIPHENYL-AMINE(65178-51-0)
• EPA Substance Registry System: ALLYL-DIPHENYL-AMINE(65178-51-0)

Safety Data

• Hazardous Substances Data: 65178-51-0(Hazardous Substances Data)

Usage

Chemical compound

ALLYL-DIPHENYL-AMINE

Physical properties

Colorless to yellow liquid with a faint odor

Solubility

Insoluble in water, soluble in organic solvents

Uses

Stabilizer and inhibitor for polymerization reactions, corrosion inhibitor for metals, intermediate in the production of dyes, pharmaceuticals, and other organic compounds

Toxicity

Low acute toxicity, potential for skin, eye, and respiratory irritation with long-term exposure; harmful if swallowed or inhaled

Precautions

Take precautions to minimize exposure

Upstream product

• 1469-70-1 allyl ethyl carbonate 
• 122-39-4 diphenylamine 
• 5162-44-7 1-bromo-4-butene 
• 106-95-6 allyl bromide 
• 589-09-3 N-allyl-N-phenylamine 
• 66003-78-9 triphenylsulfonium trifluoromethanesulfonate 
• 109-72-8 n-butyllithium 
• 591-87-7 Allyl acetate 
• 107-18-6 allyl alcohol 
• 107-05-1 3-chloroprop-1-ene 
• 623-26-7 terephthalonitrile radical anion 
• 7575-57-7 allyl benzenesulfonate 

Downstream Products

• 111-71-7 heptanal 
• 207669-94-1 4-[N-allyl-N-(4-formylphenyl)amino]benzaldehyde 
• 16292-17-4 bis(4-bromophenyl)amine 

Relevant articles and documents

DMSO-allyl bromide: A mild and efficient reagent for atom economic one-pot: N -allylation and bromination of 2°-aryl amines, 2-aryl aminoamides, indoles and 7-aza indoles

A mixture DMSO-allyl bromide has been developed as a reagent for an atom economic one-pot N-allylation and aryl bromination under basic conditions. Utilizing this reagent, N-allylation-bromination of a number of 2°-aryl amines, aryl aminoamides, indoles, and 7-aza indoles has been achieved. The scope of the substrates and limitations, the synthetic utility of the products, and a plausible reaction mechanism have been proposed.

Photophysical and electrochemical investigation of highly conjugated pyridine based diphenylamine materials

Three simple and small donor-acceptor type conjugated moieties, namely (2Z, 2′Z)-3,3'-((hexylazanediyl)bis (4,1-phenylene))bis (2-(pyridin-2-yl)acrylonitrile) (DPA-PA-1), (2Z, 2′Z)-3,3'-((dodecylazanediyl)bis (4,1-phenylene))bis (2-(pyridin-2-yl)acrylonit

Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates in water

The activation of C-O bonds in allylic acetates in water as a suspension medium has been accelerated by carrying out the reactions in the presence of platinum complexes associated with ligands. The platinum-catalyzed allylation of aminonaphthalenes using allylic acetates gave the corresponding N-allylic aminonaphthalenes in good yields.