41833-57-2

Basic information

• Product Name: 3-[(4-CHLOROPHENYL)AMINO]PROPANENITRILE
• Synonyms: 3-(4-chloroanilino)propanenitrile
• CAS NO: 41833-57-2
• Molecular Formula: C₉H₉ClN₂
• Molecular Weight: 180.6342
• Mol File: 41833-57-2.mol
• Article Data: 18

Chemical Properties

• Melting Point: 72-73 °C(Solv: ethanol (64-17-5))
• Boiling Point: 381.3 °C at 760 mmHg
• Flash Point: 184.4 °C
• Appearance: /
• Density: 1.226 g/cm³
• Vapor Pressure: 5.14E-06mmHg at 25°C
• Refractive Index: 1.593
• PKA: 3.08±0.50(Predicted)
• CAS DataBase Reference: 3-[(4-CHLOROPHENYL)AMINO]PROPANENITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(4-CHLOROPHENYL)AMINO]PROPANENITRILE(41833-57-2)
• EPA Substance Registry System: 3-[(4-CHLOROPHENYL)AMINO]PROPANENITRILE(41833-57-2)

Safety Data

• Hazardous Substances Data: 41833-57-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H9ClN2/c10-8-2-4-9(5-3-8)12-7-1-6-11/h2-5,12H,1,7H2

Upstream product

• 106-47-8 4-chloro-aniline 
• 107-13-1 acrylonitrile 
• 1075-76-9 N-cyanoethylaniline 
• 5198-49-2 3-(4-chloro-phenyl)-oxazolidin-2-one 
• 5351-04-2 3-diethylaminopropionitrile 
• 20265-96-7 p-chloroaniline hydrochloride 

Downstream Products

• 55240-19-2 C₁₀H₈Cl₂N₂O 
• 190843-15-3 N-(4-chlorophenyl)-N-(4-oxo-4H-pyrido[3,2-e]-1,3-thiazin-2-yl)-3-aminopropionitrile 
• 55246-83-8 C₁₀H₈Cl₂N₂S 
• 21617-19-6 3-(4-chlorophenylamino)propionic acid 

Relevant articles and documents

Halogenated method of aromatic compound

The invention belongs to the field of organic synthesis, and particularly relates to synthesis of aromatic halogens, in particular to arylamine. The invention discloses a synthesis method of a corresponding ortho-halogenated product from aromatic compounds such as carbazole and phenol. The method comprises the following steps: adding a metal sulfonate salt catalyst, aromatic amine, carbazole, phenol and other hydrogen - heteroatom-containing aromatic compound reaction substrates, a halogenation reagent and a reaction solvent at a specific reaction temperature. After the drying agent is dried, the yield of the reaction product and the nuclear magnetic characterization determining structure are determined by column chromatography. The reaction product yield is determined by gas chromatography. By adopting the method, under the cheap metal salt catalyst, a plurality of ortho-substituted brominated and chloro products can be obtained with moderate to excellent yield.

Polymer coated magnetically separable organocatalyst for C[sbnd]N bond formation via aza-Michael addition

A polyacrylamide coated magnetite (PAM@MNP) catalyst was synthesized by following a two step approach involving the reaction of magnetite (Fe3O4) particles with coupling agent 3-(trimethoxysilyl)propyl methacrylate followed by grafting of acrylamide and subsequent polymerization via surface initiated radical polymerization technique. The synthesized organocatalyst was used for a one-pot aza-Michael addition reaction of amines with electron deficient alkenes to give β-amino carbonyls. The magnetic properties of the synthesized organocatalyst provide it a facile recovery by external magnet which eliminates the problems arising during catalyst separation by conventional filtration.

Boric acid/glycerol as an efficient catalyst for synthesis of thiomorpholine 1,1-dioxide by double michael addition reaction in water

Thiomorpholine 1,1-dioxides were prepared with double Michael addition reaction of aromatic amines to divinyl sulfone catalyzed by boric acid/glycerol in water. This catalyst system was also used for the Michael addition reaction of aromatic amines to electron-deficient alkenes. The reaction is simple and green and gives good to excellent yields.