2968-13-0

Basic information

• Product Name: (4-FLUOROPHENYLTHIO)ACETONE
• Synonyms: (4-FLUOROPHENYLTHIO)ACETONE;(4-FLUOROPHENYLTHIO)-N-PROPAN-2-ONE;(4-FLUOROPHENYLTHIO)PROPAN-2-ONE;(4-Fluorophenylthio)propan-2-one 97%;(4-Fluorophenylthio)propan-2-one97%;1-[(4-fluorophenyl)thio]acetone;1-(4-fluorophenylthio)propan-2-one
• CAS NO: 2968-13-0
• Molecular Formula: C₉H₉FOS
• Molecular Weight: 184.23
• Mol File: 2968-13-0.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 100-103°C 1mm
• Flash Point: 100-103°C/1mm
• Appearance: /
• Sensitive: Stench
• CAS DataBase Reference: (4-FLUOROPHENYLTHIO)ACETONE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-FLUOROPHENYLTHIO)ACETONE(2968-13-0)
• EPA Substance Registry System: (4-FLUOROPHENYLTHIO)ACETONE(2968-13-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 2968-13-0(Hazardous Substances Data)

Usage

General Description

(4-Fluorophenylthio)acetone is a synthetic chemical compound. The chemical formula for this substance is C9H9FO, suggesting it comprises nine atoms of carbon, nine atoms of hydrogen, one of fluorine, and one of oxygen. It belongs to the group of organofluorines. This generally indicates a family of organic compounds that contain fluorine. The chemical structure of (4-Fluorophenylthio)acetone consists of a four-position fluorophenylthio group attached to an acetone molecule. Like many other chemicals, it is likely utilized in various industrial and research applications, although detailed information about this specific compound may be limited, as it is quite specialized. It should be handled with care, as with any chemical, to prevent unwanted reactions or dangers.

Upstream product

• 371-42-6 4-Fluorothiophenol 
• 78-95-5 chloroacetone 
• 3887-61-4 sodium 4-fluorophenylthiolate 
• 108-22-5 Isopropenyl acetate 
• 405-31-2 bis(4-fluorophenyl)disulfide 
• 67-64-1 acetone 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 

Downstream Products

• 691357-04-7 6,7-difluoro-2-(4-fluoro-phenylsulfanyl)-3-methyl-quinoxaline 1,4-dioxide 
• 820975-39-1 2-(5-fluoro-2-(4-fluorophenylthio)benzo[b]thiophen-3-yl)acetonitrile 
• 820975-37-9 3-(bromomethyl)-5-fluoro-2-(4-fluorophenylthio)benzo[b]thiophene 
• 820975-38-0 5-fluoro-2-(4-fluorophenylthio)-3-methylbenzo[b]thiophene 
• 432-98-4 1-(4-fluorophenylsulfonyl)propan-2-one 
• 675185-74-7 5-{[(4-fluorophenyl)sulphanyl]methyl}-5-methylimidazolidine-2,4-dione 
• 397330-28-8 2-acetylamino-2-methyl-3-(4-phenylsulfanyl-benzenesulfonyl)-propionic acid 
• 404963-90-2 TY-51076 
• 404964-34-7 5-fluoro-2-chlorosulfonyl-3-methylbenzo[b]thiophene 
• 212078-55-2 (E)-1-(5-fluoro-3-methylbenzo[b]thiophen-2-yl)-3-(1-triphenylmethyl-1H-imidazol-4-yl)-2-propen-1-one 
• 212078-57-4 1-(5-fluoro-3-methylbenzo[b]thiophen-2-yl)-3-(1-triphenylmethyl-1H-imidazol-4-yl)propan-1-ol 
• 51828-34-3 2-acetyl-5-fluoro-3-methylbenzo[b]thiophene 

Relevant articles and documents

Synthesis of α-arylthioacetones using TEMPO as the: C 3 synthon via a reaction cascade of sequential oxidation, skeletal rearrangement and C-S bond formation

Here, we present an unprecedented pathway to α-sulfenylated carbonyl compounds from commercially available thiols and universally employed TEMPO and its analogues, which act as C3 synthons through skeletal rearrangement under simple and metal-f

A sulfur-containing amino acid amide carbamate derivative and application thereof

The invention belongs to the field of plant fungicides, and relates to sulfur-containing amino acid amide carbamate derivatives of which the general formulas I are shown in the description and pharmaceutically acceptable salts of the sulfur-containing amino acid amide carbamate derivatives. In the general formulas I, substituent groups R1, R2 and n are defined in the description. The invention further relates to preparation methods of compounds related to the general formulas I, special intermediates developed for the preparation of the compounds, and application of the compounds to prevention and control of plant diseases.

Electrophilic substitution reactions using an electrogenerated ArS(ArSSAr)+ cation pool as an ArS+ equivalent

Arylbis(arylthio)sulfonium ions (ArS(ArSSAr)+), which were generated and accumulated by the low-temperature electrolysis of diaryl disulfide (ArSSAr), were found to serve as ArS+ equivalent in electrophilic substitution reactions of