79807-20-8

Basic information

• Product Name: (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone
• CAS NO: 79807-20-8
• Molecular Formula: C₁₄H₉Cl₂NO
• Molecular Weight: 278.1334
• Mol File: 79807-20-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 425.7°C at 760 mmHg
• Flash Point: 167.7°C
• Density: 1.25g/cm³
• Vapor Pressure: 1.88E-07mmHg at 25°C
• Refractive Index: 1.592
• CAS DataBase Reference: (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone(79807-20-8)
• EPA Substance Registry System: (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone(79807-20-8)

Safety Data

• Hazardous Substances Data: 79807-20-8(Hazardous Substances Data)

Usage

Description

(2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone is a chemical compound characterized by its molecular formula C15H11Cl2NO. It features an imine functional group, which is a carbon-nitrogen double bond that is connected to both a phenyl and a dichlorophenyl group. (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone is recognized for its potential in organic synthesis and pharmaceutical research, where it serves as a valuable building block for the creation of more complex molecules. Its unique structural and chemical attributes also suggest that it could be instrumental in the development of novel drugs or materials.

Uses

Used in Organic Synthesis:
(2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone is utilized as a key intermediate in organic synthesis for the preparation of a variety of complex organic molecules. Its imine functional group allows for versatile chemical reactions, making it a preferred choice for constructing intricate molecular structures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone is employed as a building block for the synthesis of new drug candidates. Its unique chemical properties and structural features make it a promising starting point for the development of innovative therapeutic agents.
Used in Material Science:
Due to its structural and chemical properties, (2E)-2-[(3,4-dichlorophenyl)imino]-1-phenylethanone may also find applications in material science. It could be used to develop new materials with specific properties, such as improved stability, reactivity, or other characteristics that are beneficial for various industrial applications.

Upstream product

• 79807-21-9 3,4-dichloro-N-(α-methoxyphenacyl)aniline 
• 1074-12-0 phenylglyoxal hydrate 

Downstream Products

• 79807-24-2 3,4-dichloro-N-(α-acetamidophenacyl)aniline 
• 79807-21-9 3,4-dichloro-N-(α-methoxyphenacyl)aniline 
• 79807-22-0 diethyl α-<(3,4-dichloroanilino)phenacyl>malonate 
• 79807-37-7 [2-(3,4-Dichloro-phenyl)-2-aza-bicyclo[2.2.1]hept-5-en-3-yl]-phenyl-methanone 
• 79807-41-3 2-(3,4-dichloroanilino)-1-phenylethanol 
• 79807-29-7 1,2-dibenzoyl-1,2-di(3,4-dichloroanilino)ethylene 
• 79807-25-3 [2-(3,4-Dichloro-phenyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-yl]-phenyl-methanone 
• 79807-27-5 [6-(3,4-Dichloro-phenyl)-6-aza-bicyclo[3.2.2]nona-3,8-dien-7-yl]-phenyl-methanone 
• 79807-44-6 2-benzoyl-1-<(3,4-dichloro)phenyl>-4,5-dimethyl-1,2,3,6-tetrahydropyridine 

Relevant articles and documents

Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 4. Synthesis of Phenylglyoxal Imine Monomers

Syntheses and reactions of N-tosylphenacylamines with bases have been systematically examined.Monomeric C-methoxy-imines are available from some of these reactions.C-Methoxyphenacylarylamines, made by two routes, were converted into monomeric imines on treatment with noble-metal catalysts, The boron trifluoride-catalysed reactions of aryl aldehydes with sulphonamides provide a new and convenient route to N-sulphonylarylimines.