4170-80-3

Basic information

• Product Name: (ethylsulfinyl)benzene
• Synonyms: benzene, (ethylsulfinyl)-; ethyl phenyl sulfoxide; Ethylphenylsulfoxide
• CAS NO: 4170-80-3
• Molecular Formula: C₈H₁₀OS
• Molecular Weight: 154.2294
• Mol File: 4170-80-3.mol
• Article Data: 255

Chemical Properties

• Boiling Point: 283.9°C at 760 mmHg
• Flash Point: 125.5°C
• Density: 1.15g/cm³
• Vapor Pressure: 0.00526mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: (ethylsulfinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (ethylsulfinyl)benzene(4170-80-3)
• EPA Substance Registry System: (ethylsulfinyl)benzene(4170-80-3)

Safety Data

• Hazardous Substances Data: 4170-80-3(Hazardous Substances Data)

Usage

General Description

(Ethylsulfinyl)benzene, also known as ethyl phenyl sulfoxide, is a chemical compound with the molecular formula C8H10OS. It is a sulfoxide compound, which means it contains a sulfur atom bonded to two organic groups and an oxygen atom. (Ethylsulfinyl)benzene is commonly used as an intermediate in the production of pharmaceuticals and organic compounds. It has also been studied for its potential antimicrobial and antioxidant properties. The compound is typically a colorless to pale yellow liquid with a characteristic odor. It is important to handle (ethylsulfinyl)benzene with caution, as it can be irritating to the skin, eyes, and respiratory system.

Upstream product

• 618-41-7 Benzenesulfinic acid 
• 4972-29-6 benzenesulphinyl chloride 
• 141-52-6 sodium ethanolate 
• 87905-04-2 (+/-)-2-(ethylsulfinyl)pyridine 
• 100-58-3 phenylmagnesium bromide 
• 7601-90-3 perchloric acid 
• 64-17-5 ethanol 
• 622-38-8 Ethyl phenyl sulfide 
• 7722-84-1 dihydrogen peroxide 
• 925-90-6 ethylmagnesium bromide 
• 98-09-9 benzenesulfonyl chloride 
• 26910-34-9 α-Bromoethyl phenyl sulfoxide 
• 5467-74-3 4-Bromophenylboronic acid 
• 98-80-6 phenylboronic acid 

Downstream Products

• 882-33-7 diphenyldisulfane 
• 622-38-8 Ethyl phenyl sulfide 
• 156082-33-6 C₁₄H₁₄OSSe 
• 51207-25-1 (R)-ethyl phenyl sulfoxide 
• 71369-95-4 2-(1-phenylthioethyl)cyclohexanone 
• 69765-77-1 (+/-)-S-ethyl-S-phenyl-N-[(p-tolyl)sulfonyl]sulfoximid 
• 4170-80-3 (S)-(-)-ethylphenylsulfoxide 
• 599-70-2 ethyl phenyl sulfone 
• 1308853-75-9 ethyl 1-(2-(ethylthio)phenyl)-2-oxocyclohexanecarboxylate 
• 121034-19-3 (phenyl)(ethyl)(imino)-λ⁶-sulfanone 
• 92050-37-8 (2-phenoxyphenyl)(phenyl)sulfane 

Relevant articles and documents

Chiral Ligands in Hypervalent Iodine Compounds: Synthesis and Structures of Binaphthyl-Based λ3-Iodanes

Several novel binaphthyl-based chiral hypervalent iodine(III) reagents have been prepared and structurally analysed. Various asymmetric oxidative reactions were applied to evaluate the reactivities and stereoselectivities of those reagents. Moderate to excellent yields were observed; however, very low stereoselectivities were obtained. NMR experiments indicated that these reagents are very easily hydrolysed in either chloroform or DMSO solvents leading to the limited stereoselectivities. It is concluded that the use of chiral ligands is an unsuccessful way to prepare efficient stereoselective iodine(III) reagents.

Synthesis and characterization of magnetic Fe3O4@Creatinine@Zr nanoparticles as novel catalyst for the synthesis of 5-substituted 1H-tetrazoles in water and the selective oxidation of sulfides with classical and ultrasonic methods

Tetrazoles and sulfoxide compounds have a wide range of applications in industries and are of great expectation to be environmentally friendly and cost-effective. This paper reports the introduction of zirconium supported on Fe3O4 na

Assembly of polyoxometalate-thiacalix[4]arene-based inorganic-organic hybrids as efficient catalytic oxidation desulfurization catalysts

Self-assembly of polyoxometalates, Ni(ii)/Ag(i) cations and tetra-[5-(mercapto)-1-methyltetrazole]-thiacalix[4]arene (L) yielded three inorganic-organic hybrids, namely, [Ni3L2(CH3OH)6(H2O)4][PMo12O40]2·3CH3OH·2H2O (1), [Ni3L2(CH3OH)6(H2O)4][PW12O40]2·3CH3OH·2H2O (2) and [Ag3L(PMo12O40)] (3). In hybrids (1) and (2), Ni(ii) cations are linked by L ligands to produce layered frameworks, and H bonds among the [PMo12O40]3?/[PW12O40]3?anions and L ligands lengthen the structures to form 3D supramolecular architectures. Hybrid (3) exhibits a 3D architecture, of which Ag(i) cations not only coordinated with the N and O atoms of L ligands and [PMo12O40]3?anions simultaneously, but also connected each other by Ag-Ag interactions. It is worth mentioning that1and3as recyclable catalysts show excellent heterogeneous catalytic activity in oxidation desulfurization reactions.