802-49-3

Basic information

• Product Name: 1-Propanone, 3-[(4-methoxyphenyl)amino]-1,3-diphenyl-
• CAS NO: 802-49-3
• Molecular Formula: C22H21NO2
• Molecular Weight: 331.414
• Mol File: 802-49-3.mol
• Article Data: 74

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-[(4-methoxyphenyl)amino]-1,3-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-[(4-methoxyphenyl)amino]-1,3-diphenyl-(802-49-3)
• EPA Substance Registry System: 1-Propanone, 3-[(4-methoxyphenyl)amino]-1,3-diphenyl-(802-49-3)

Safety Data

• Hazardous Substances Data: 802-49-3(Hazardous Substances Data)

Usage

Structure

A propane backbone with two phenyl groups and an amino group attached to the third carbon atom, and a methoxy group attached to one of the phenyl groups.

Type of compound

Ketone derivative

Usage

Building block for organic synthesis and pharmaceutical research.

Potential applications

Range of applications due to its structural properties and unique reactivity.

Upstream product

• 13735-81-4 1-styrenyloxytrimethylsilane 
• 1613-90-7 4-methoxy-N-[(E)-phenylmethylidene]aniline 
• 536-90-3 m-Anisidine 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 
• 104-94-9 4-methoxy-aniline 
• 40339-42-2 4-methoxy-N-[(1Z)-phenylmethylene]aniline 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 94-41-7 benzalacetophenone 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 614-47-1 1,3-diphenyl-propen-3-one 

Relevant articles and documents

Tuning Microenvironment of Quaternary Ammonium Salt and Tertiary Amine Bifunctionalized Polyacrylonitrile Fiber for Cooperatively Catalyzed Aza-Michael Addition

A series of novel polyacrylonitrile fiber catalysts modified with different ratio of quaternary ammonium salt (QA) to tertiary amine (TA) were screened for heterogeneously catalyzed aza-Michael addition in water. The best catalyst was found to be PAN

An uncommon use of irradiated flavins: Br?nsted acid catalysis

We present that thioacetalization of aldehydes can be induced by blue light irradiation in the presence of a catalytic amount of riboflavin tetraacetate (RFTA) under aerobic conditions. Several control experiments have suggested that the reaction is more

Ionic liquid-immobilized proline(s) organocatalyst-catalyzed one-pot multi-component Mannich reaction under solvent-free condition

A highly efficient clean and simple methodology has been established for the one-pot Mannich reaction using ionic liquid-immobilized proline(s) organocatalyst under solvent-free conditions. The three components comprising substituted acetophenones, substituted aromatic aldehydes and substituted aromatic amines underwent Mannich reactions in the presence of 7?mol% of ionic liquid-immobilized proline(s) organocatalyst to provide β-amino carbonyl compounds in 2–3?h at room temperature with excellent yields. This methodology provides several advantages such as mild reaction conditions, short reaction time, low catalyst loading percentage, multi-component approach, transition metal-free and solvent-free synthesis. The ionic liquid-immobilized proline(s) organocatalyst was recycled and reused five times without a significant loss of its catalytic activity.