29193-63-3

Basic information

• Product Name: 4-(4-CHLORO-PHENYLSULFANYL)-BUTYRIC ACID
• Synonyms: 4-[(4-chlorophenyl)thio]butanoic acid
• CAS NO: 29193-63-3
• Molecular Formula: C₁₀H₁₁ClO₂S
• Molecular Weight: 230.71
• Mol File: 29193-63-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 394oC at 760 mmHg
• Flash Point: 192.1oC
• Appearance: /
• Density: 1.31g/cm³
• Vapor Pressure: 6.49E-07mmHg at 25°C
• Refractive Index: 1.595
• PKA: 4.62±0.10(Predicted)
• CAS DataBase Reference: 4-(4-CHLORO-PHENYLSULFANYL)-BUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-CHLORO-PHENYLSULFANYL)-BUTYRIC ACID(29193-63-3)
• EPA Substance Registry System: 4-(4-CHLORO-PHENYLSULFANYL)-BUTYRIC ACID(29193-63-3)

Safety Data

• Hazardous Substances Data: 29193-63-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H11ClO2S/c11-8-3-5-9(6-4-8)14-7-1-2-10(12)13/h3-6H,1-2,7H2,(H,12,13)

Upstream product

• 96-48-0 4-butanolide 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 29107-85-5 ethyl 4-((4-chlorophenyl)thio)butanoate 
• 2623-87-2 bromobutyric acid 
• 106-54-7 p-Chlorothiophenol 
• 18803-44-6 sodium p-chlorothiophenolate 

Downstream Products

• 30484-10-7 7-Chloro-2,3,4,5-tetrahydro-1-benzothiepin-5-one 
• 61016-63-5 Sodium 4-(p-Chlorophenylthio)butyrate 
• 61797-42-0 4-(4-Chloro-phenylsulfanyl)-N-(2-{[4-(4-chloro-phenylsulfanyl)-butyryl]-methyl-amino}-ethyl)-N-methyl-butyramide 
• 114302-74-8 Carboxydimethylmethyl--sulfoxid 
• 29193-68-8 4-<4-Chlor-benzolsulfonyl>-buttersaeure 

Relevant articles and documents

Production of Alkyl Aryl Sulfides from Aromatic Disulfides and Alkyl Carboxylates via a Disilathiane–Disulfide Interchange Reaction

The results of this study show that disilathiane is an effective mediator in the synthesis of alkyl aryl sulfides with disulfides and alkyl carboxylates. Mechanistic studies suggest that disilathiane promotes cleavage of the sulfur–sulfur bond of disulfides to generate thiosilane as a key intermediate. Diselenides were also applicable to this transformation to produce the corresponding selenides.

Thiochroman-4-one thiosemicarbazide compound as well as preparation method and application thereof

The invention relates to a thiochroman-4-one thiosemicarbazide compound, as well as a preparation method and an application thereof. The structural formula of the thiochroman-4-one thiosemicarbazide compound is shown as Formula (I), wherein n is 1 or 2, R