658-14-0

Basic information

• Product Name: 1-Fluoro-4-(methylsulfinyl)benzene
• Synonyms: 1-Fluoro-4-(methylsulfinyl)benzene;1-FLUORO-4-(METHYLSULFINYL)BENZENE(WXC09195)
• CAS NO: 658-14-0
• Molecular Formula: C₇H₇FOS
• Molecular Weight: 158.1932832
• Mol File: 658-14-0.mol
• Article Data: 126

Chemical Properties

• Boiling Point: 264.9±23.0 °C(Predicted)
• Appearance: /
• Density: 1.29±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1-Fluoro-4-(methylsulfinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Fluoro-4-(methylsulfinyl)benzene(658-14-0)
• EPA Substance Registry System: 1-Fluoro-4-(methylsulfinyl)benzene(658-14-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 658-14-0(Hazardous Substances Data)

Usage

General Description

1-Fluoro-4-(methylsulfinyl)benzene is a chemical compound with the molecular formula C7H7FS. It is an aromatic compound with a single fluorine atom and a methylsulfinyl group attached to a benzene ring. 1-Fluoro-4-(methylsulfinyl)benzene is commonly used in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. It has also been studied for its potential applications in materials science and as a precursor for the synthesis of other fluorinated compounds. 1-Fluoro-4-(methylsulfinyl)benzene is a versatile and useful chemical compound with a wide range of potential industrial applications.

Upstream product

• 371-15-3 p-fluorothioanisole 
• 100-68-5 methyl-phenyl-thioether 
• 3996-46-1 p-FC₆H₄SOCH₂COOH 
• 371-42-6 4-Fluorothiophenol 
• 332-51-4 (4-fluorophenylthio)acetic acid 
• 67-68-5 dimethyl sulfoxide 
• 164021-74-3 (1S,2R)-(-)-2-[N-(3’,5’-di-tert-butylsalicylidene)amino]-1,2-diphenylethanol 

Downstream Products

• 455-15-2 1-(methylsufonyl)-4-fluorobenzene 
• 371-15-3 p-fluorothioanisole 
• 635311-89-6 (4-fluorophenyl)(imino)(methyl)-λ⁶-sulfanone 
• 635311-88-5 C₁₃H₂₂FNOSSi 
• 635311-90-9 C₄₇H₈₂FNO₃SSi₃ 
• 1426131-98-7 1-(tert-butyl)-4-(((4-fluorophenyl)sulfinyl)methyl)benzene 
• 39547-79-0 1-fluoro-4-((fluoromethyl)sulfonyl)benzene 
• 658-14-0 R-(-)-4-fluoro phenyl methyl sulfoxide 
• 175911-67-8 S-(+)-4-fluoro phenyl methyl sulfoxide 
• 226396-70-9 (4-fluoro-phenylsulfanyl)-acetic acid methyl ester 

Relevant articles and documents

Visible light-promoted selective oxidation of sulfides to sulfoxides catalyzed by ruthenium porphyrins with iodobenzene diacetate

Under visible light irradiation, the carbonyl ruthenium(II) porphyrin complexes efficiently catalyze the selective oxidation of sulfides to sulfoxides with iodobenzene diacetate [PhI(OAc)2] as the oxygen source. Various thioanisoles and allylic

VpStyA1/VpStyA2B of variovorax paradoxus EPS: An aryl alkyl sulfoxidase rather than a styrene epoxidizing monooxygenase

Herein we describe the first representative of an E2-type two-component styrene monooxygenase of proteobacteria. It comprises a single epoxidase protein (VpStyA1) and a two domain protein (VpStyA2B) harboring an epoxidase (A2) and a FAD-reductase (B) doma

Synthesis method of sulfoxide compound

The invention discloses a method for preparing sulfoxide derivatives with industrial application value through substituted diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds. Under electrochemical reaction conditions, diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfide compounds which are wide in source and easy to prepare and have structural diversity are used as raw materials, lithium perchlorate (LiClO4) is used as an electrolyte, acetonitrile (CH3CN) is used as a solvent, and oxygen is used as an oxidizing agent to prepare the diaryl (heterocyclic aryl) and aryl (heterocyclic aryl) alkyl sulfoxide derivatives. Compared with reported preparation methods of sulfoxide derivatives, the preparation method disclosed by the invention is green, environment-friendly, safe, energy-saving, wide in substrate application range, good in compatibility of product functional groups, easy in obtaining of raw materials and simple and convenient to operate.

Synergistic cooperative effect of CF3SO2Na and bis(2-butoxyethyl)ether towards selective oxygenation of sulfides with molecular oxygen under visible-light irradiation

A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF3SO2Na and 2-butoxyethyl ether represents the key promoting factor for the reaction. This journal is

Sulfoxide and Sulfone Synthesis via Electrochemical Oxidation of Sulfides

The oxidation of diaryl sulfides and aryl alkyl sulfides to the corresponding sulfoxides and sulfones under electrochemical conditions is reported. Sulfoxides are selectively obtained in good yield under a constant current of 5 mA for 10 h in DMF, while sulfones are formed as the major product under a constant current of 10 or 20 mA for 10 h in MeOH. The oxygen of both the sulfoxide and sulfone function is derived from water.