338953-54-1

Basic information

• Product Name: (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE
• Synonyms: (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE;(3-chloro-5-(trifluoromethyl)pyridin-2-yl)(4-chlorophenyl)methanone
• CAS NO: 338953-54-1
• Molecular Formula: C13H6Cl2F3NO
• Molecular Weight: 320.09
• Mol File: 338953-54-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 376.0±42.0 °C(Predicted)
• Appearance: /
• Density: 1.467±0.06 g/cm3(Predicted)
• PKA: -2.33±0.10(Predicted)
• CAS DataBase Reference: (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE(338953-54-1)
• EPA Substance Registry System: (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE(338953-54-1)

Safety Data

• Hazardous Substances Data: 338953-54-1(Hazardous Substances Data)

Usage

General Description

The chemical compound "(4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE" is a member of the aryl ketone class of compounds. It is characterized by the presence of a chlorophenyl group attached to a 3-chloro-5-(trifluoromethyl)-2-pyridinyl moiety through a methanone linker. (4-CHLOROPHENYL)[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE may have applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its potential as a building block for the synthesis of more complex molecules with desirable properties. However, detailed studies and evaluations of its chemical and biological properties are necessary to fully understand its potential uses and effects.

Upstream product

• 213993-80-7 C₁₄H₇Cl₂F₃N₂ 
• 104-88-1 4-chlorobenzaldehyde 
• 69045-84-7 2,3-dichloro-5-trifluoromethylpyridine 
• 140-53-4 p-chlorobenzyl cyanide 

Relevant articles and documents

Substituted 2-benz(o)ylpyridines, their preparation and their use as herbicides

Substituted 2-benz(o)ylpyridines I and salts thereof where n=0, 1; X=CO, CH2, CH(C1-C4-alkyl), CH—OH, CH—CN, CH-halogen, C(halogen)2, CH—CONH2, CH—CO—O(C1-C4-alkyl), CH—O(C1-C4-alkyl), C(CN)(C1-C4-alkyl); R1=halogen, C1-C4-haloalkyl, C1-C4-alkylthio, C1-C4-alkylsulfinyl, C1-C4-alkylsulfonyl; R2=H, halogen; R3=H, NO2, OH, halogen, C1-C4-alkoxy; R4=H, NO2, OH, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy; R5=H, NO2, CN, halogen, C1-C8-alkyl, C3-C8-alkenyl, C3-C8-alkynyl, C3-C8-cycloalkyl, C1-C8-haloalkyl, C2-C8-haloalkenyl, C2-C8-haloalkinyl, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkynyloxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, cyano-C2-C8-alkenyl, cyano-C3-C8-alkynyl, unsubstituted or substituted OH, SH, SO—H, —SO2—H, COOH or NH—COOH, —SO2Cl, —N(R9,R10), —NH—SO2—(C1-C8-alkyl), —N[—SO2—(C1-C8-alkyl)]2, —N(C1-C8-alkyl)[—SO2—(C1-C8-alkyl)], —SO2—N(R9,R10), —O—CO—NH—R9, unsubstituted or substituted CHO, —O—CHO or —NH—CHO, —NH—CO—NH—R9, —O—CS—NH2, —O—CS—N(C1-C8-alkyl)2, —CO—N(R9,R10), —CS—N(R9,R10), —CO—NH—SO2—(C1-C4-alkyl).