213993-80-7

Basic information

• Product Name: 2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]ACETONITRILE
• Synonyms: 2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]ACETONITRILE;2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)PYRID-2-YL]ACETONITRILE;2-(4-CHLOROPHENOL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)PYRID-2-YL]ACETONITRILE;2-(4-Chlorophenyl)-2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrile97%
• CAS NO: 213993-80-7
• Molecular Formula: C₁₄H₇Cl₂F₃N₂
• Molecular Weight: 331.12
• Mol File: 213993-80-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 47-49°C
• Boiling Point: 146°C 0,1mm
• Appearance: /
• CAS DataBase Reference: 2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]ACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]ACETONITRILE(213993-80-7)
• EPA Substance Registry System: 2-(4-CHLOROPHENYL)-2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]ACETONITRILE(213993-80-7)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 213993-80-7(Hazardous Substances Data)

Usage

Type of compound

Nitrile derivative

Usage

Organic synthesis, building block for pharmaceuticals and agrochemicals

Physical state

White solid

Water solubility

Sparingly soluble

Solubility in organic solvents

Soluble

Potential environmental impact

Pollutant (low water solubility, potential toxicity)

Handling and disposal

Follow safety protocols and regulatory guidelines to minimize impact on human health and the environment

Upstream product

• 69045-84-7 2,3-dichloro-5-trifluoromethylpyridine 
• 140-53-4 p-chlorobenzyl cyanide 

Downstream Products

• 213993-82-9 C₁₄H₉Cl₂F₃N₂O 
• 338953-54-1 C₁₃H₆Cl₂F₃NO 

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).