112446-18-1

Basic information

• Product Name: 1-{5-chloro-2-[(3,4-dichlorophenyl)sulfanyl]phenyl}ethanone
• Synonyms: 1-{5-chloro-2-[(3,4-dichlorophenyl)sulfanyl]phenyl}ethanone
• CAS NO: 112446-18-1
• Molecular Formula: C₁₄H₉Cl₃OS
• Molecular Weight: 331.64466
• Mol File: 112446-18-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-{5-chloro-2-[(3,4-dichlorophenyl)sulfanyl]phenyl}ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{5-chloro-2-[(3,4-dichlorophenyl)sulfanyl]phenyl}ethanone(112446-18-1)
• EPA Substance Registry System: 1-{5-chloro-2-[(3,4-dichlorophenyl)sulfanyl]phenyl}ethanone(112446-18-1)

Safety Data

• Hazardous Substances Data: 112446-18-1(Hazardous Substances Data)

Usage

Type of compound

Ketone

Structure

a. Chloro-substituted phenyl ring
b. Dichlorophenylsulfanyl group attached to the phenyl ring

Industry use

Pharmaceutical industry

Applications

a. Synthesis of various drugs
b. Pharmaceutical intermediates
c. Potential applications in organic synthesis and chemical research

Specific properties and uses

Depend on the specific application and conditions under which it is used

Upstream product

• 2476-37-1 2,5-dichloroacetophenone 
• 5858-17-3 3,4-dichlorothiophenol 

Downstream Products

• 112446-46-5 1-{1-[5-Chloro-2-(3,4-dichloro-phenylsulfanyl)-phenyl]-ethyl}-4-(3-chloro-phenyl)-piperazine 
• 112446-43-2 1-{1-[5-Chloro-2-(3,4-dichloro-phenylsulfanyl)-phenyl]-ethyl}-4-phenyl-piperazine 
• 112446-39-6 1-{1-[5-Chloro-2-(3,4-dichloro-phenylsulfanyl)-phenyl]-ethyl}-4-(2-methoxy-ethyl)-piperazine 
• 112446-37-4 2-(4-{1-[5-Chloro-2-(3,4-dichloro-phenylsulfanyl)-phenyl]-ethyl}-piperazin-1-yl)-ethanol 
• 112446-33-0 1-{1-[5-Chloro-2-(3,4-dichloro-phenylsulfanyl)-phenyl]-ethyl}-4-methyl-piperazine 
• 112446-28-3 C₁₄H₁₀Cl₄S 
• 112446-23-8 1-(5-chloro-2-(3,4-dichlorophenylthio)phenyl)ethanol 

Relevant articles and documents

4-SUBSTITUTED 1-(1-(2-(ARYLTHIO)-5-HALOGENOPHENYL)ETHYL)PIPERAZINES; SYNTHESIS AND BIOLOGICAL SCREENING

Reactions of 2,5-dichloroacetophenone and 2,5-dibromoacetophenone with a series of thiophenols gave the 2-(arylthio)-5-halogenoacetophenones VII and VIII which were reduced with sodium borohydride in ethanol to the secondary alcohols IX and X.Treatment wi