69962-41-0

Basic information

• Product Name: 3-(N,N-Diallyl)aminoacetanilide
• Synonyms: 3-(N,N-DIALLYL)AMINO ACETANILIDE;N,N-DIALLYL-3-AMINOACETANILIDE;3-(Diallylamino)acetanilide
• CAS NO: 69962-41-0
• Molecular Formula: C₁₄H₁₈N₂O
• Molecular Weight: 230.31
• Mol File: 69962-41-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 1.062
• Refractive Index: 1.587
• CAS DataBase Reference: 3-(N,N-Diallyl)aminoacetanilide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N,N-Diallyl)aminoacetanilide(69962-41-0)
• EPA Substance Registry System: 3-(N,N-Diallyl)aminoacetanilide(69962-41-0)

Safety Data

• Hazardous Substances Data: 69962-41-0(Hazardous Substances Data)

Usage

General Description

3-(N,N-Diallyl)aminoacetanilide is a chemical compound that falls under the category of organic compounds, specifically, anilides and derivatives. It is often represented by the formula C14H20N2O. 3-(N,N-Diallyl)aminoacetanilide is commonly used in research and experimental settings rather than having widespread commercial or industrial usage. However, like many chemicals, care should be taken in its handling and usage due to potential biohazard or toxicity risks. Accurate data on its specific properties, such as melting point, boiling point, and density, can vary and it's suggested to refer to the supplier's details or scientific research for precise information.

InChI:InChI=1/C14H18N2O/c1-4-9-16(10-5-2)14-8-6-7-13(11-14)15-12(3)17/h4-8,11H,1-2,9-10H2,3H3,(H,15,17)

Upstream product

• 30438-96-1 N,N-diallyl-3-nitroaniline 
• 64-19-7 acetic acid 
• 141-78-6 ethyl acetate 
• 106-95-6 allyl bromide 
• 102-28-3 m-acetamide aniline 

Downstream Products

• 184097-44-7 N-(3-(1H-pyrrol-1-yl)phenyl)acetamide 

Relevant articles and documents

A Phosphine-Mediated Dearomative Skeletal Rearrangement of Dianiline Squaraine Dyes

A phosphorus(III)-mediated dearomatization of ortho-substituted dianiline squaraine dyes results in an unusual skeletal rearrangement to provide exotic, highly conjugated benzofuranone and oxindole scaffolds bearing a C3 side chain comprised of a linear conflagration of an enol, a phosphorus ylide, and 2,4-disubstituted aniline. Employing experimental and computational analysis, a mechanistic evaluation revealed a striking dependence on the acidity of the aniline ortho substituent. Notably, the rearrangement adducts underwent rapid and complete reversion to the parent squaraine in the presence of a Br?nsted acid.

Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans

An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.