84196-19-0

Basic information

• Product Name: (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile
• Synonyms: (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile;2-Chloro-α-(4-chlorophenyl)-5-(1-methylethyl)-4-nitrobenzeneacetonitrile;Einecs 282-429-5
• CAS NO: 84196-19-0
• Molecular Formula: C₁₇H₁₄Cl₂N₂O₂
• Molecular Weight: 349.21126
• EINECS: 282-429-5
• Mol File: 84196-19-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 477.6°C at 760 mmHg
• Flash Point: 242.7°C
• Appearance: /
• Density: 1.316g/cm³
• Vapor Pressure: 2.76E-09mmHg at 25°C
• Refractive Index: 1.599
• CAS DataBase Reference: (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile(84196-19-0)
• EPA Substance Registry System: (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile(84196-19-0)

Safety Data

• Hazardous Substances Data: 84196-19-0(Hazardous Substances Data)

Usage

General Description

(2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile is a chemical compound with a complex and specific structure. It is a nitrile derivative and consists of two aromatic rings with chloro and nitro substituents, as well as an acetonitrile group. The presence of both chloro and nitro groups makes this compound potentially reactive and toxic. It may be used as an intermediate or precursor in the synthesis of pharmaceuticals, agrochemicals, or other organic compounds. Due to its specific structure and functional groups, it may have distinct chemical and physical properties that make it suitable for certain applications in organic chemistry. As with any chemical compound, proper handling and use of (2-chloro-5-isopropyl-4-nitrophenyl)(4-chlorophenyl)acetonitrile is important to ensure safety and environmental responsibility.

InChI:InChI=1/C17H14Cl2N2O2/c1-10(2)13-7-14(16(19)8-17(13)21(22)23)15(9-20)11-3-5-12(18)6-4-11/h3-8,10,15H,1-2H3

Relevant articles and documents

Antiparasitic salicylanilide derivatives

Compounds of the class of salicylanilides substituted in the 4-position of the anilino moiety with a --CH(CN)-Ar group wherein Ar is phenyl, substituted phenyl, thienyl, halothienyl or naphthalenyl, said salicylanilides being useful as parasiticides.