38452-13-0

Basic information

• Product Name: Benzene, 1-methoxy-2-(methylsulfinyl)-
• Synonyms: 2-methoxy-1-(methylsulfinyl)benzene;Methyl-(2-methoxy-phenyl)-sulfoxyd;o-anisyl methyl sulfoxide;1-methylsulfinyl-2-methoxybenzene;Benzene,1-methoxy-2-(methylsulfinyl);1-methanesulfinyl-2-methoxy-benzene;1-methoxy-2-(methylsulfinyl)benzene;2-Methoxyphenylmethylsulfoxide
• CAS NO: 38452-13-0
• Molecular Formula: C8H10O2S
• Molecular Weight: 170.232
• Mol File: 38452-13-0.mol
• Article Data: 71

Chemical Properties

• Melting Point: 44 °C
• Boiling Point: 323.8±25.0 °C(Predicted)
• Density: 1.22±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Benzene, 1-methoxy-2-(methylsulfinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-2-(methylsulfinyl)-(38452-13-0)
• EPA Substance Registry System: Benzene, 1-methoxy-2-(methylsulfinyl)-(38452-13-0)

Safety Data

• Hazardous Substances Data: 38452-13-0(Hazardous Substances Data)

Upstream product

• 144-86-5 N-chloro-4-methylbenzenesulfonamide 
• 2388-73-0 1-methoxy-2-(methylsulfanyl)benzene 
• 1073-29-6 2-(methylsulfenyl)phenol 
• 7697-37-2 nitric acid 
• 108-24-7 acetic anhydride 
• 67-56-1 methanol 
• 130922-30-4 1-fluoro-2-(methylsulfinyl)benzene 
• 139696-88-1 2-chlorophenyl methyl sulfoxide 
• 7217-59-6 2-Methoxybenzenethiol 
• 74-88-4 methyl iodide 
• 850175-28-9 3-(2-methoxyphenylsulfinyl)propionic acid ethyl ester 
• 164979-75-3 3-(2-methoxyphenylsulfanyl)propionic acid ethyl ester 

Downstream Products

• 93273-76-8 2-Cyclohexyl-1-((R)-2-methoxy-benzenesulfinyl)-propan-2-ol 
• 151042-13-6 Cr(CO)3(C₆H₄(SCH₃)OCH₃) 
• 156188-97-5 pentacarbonyl[1-methoxy-2-(methylthio)benzene-S]chromium⁽⁰⁾ 
• 14372-66-8 o-cyano-thioanisole 
• 126770-56-7 1-methoxy-2-[(2-methoxyphenyl)sulfanyl]benzene 
• 2388-73-0 1-methoxy-2-(methylsulfanyl)benzene 
• 156220-41-6 (CO)5Cr(CH₃OC₆H₄S(O)CH₃) 
• 1041856-49-8 N-(benzyloxycarbonyl)-S-methyl-S-(2-methoxyphenyl)sulfilimine 
• 84413-74-1 (R)-1-methoxy-2-(methylsulfinyl)benzene 
• 84413-73-0 (S)-(-)-2-methoxyphenyl methyl sulfoxide 
• 127642-03-9 (p-methoxyphenylsulfinyl)acetone 
• 4111-54-0 lithium diisopropyl amide 
• 208191-64-4 2-methanesulfonyl-4-nitro-phenol 

Relevant articles and documents

Hypervalent iodine(III) oxidation catalyzed by quaternary ammonium salt in miceliar systems

Catalytic activation of iodosobenzene (PhI=O) by cetyltrimethylammonium bromide (CTAB) allows sulfide oxidation reaction to occur in high yields under mild conditions in a variety of solvents. This PhI=O activation may be due to the formation of micellar

Extending aromatic acids on TiO2 for cooperative photocatalysis with triethylamine: Violet light-induced selective aerobic oxidation of sulfides

Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy. Here, the benchmark photocatalyst TiO2 was used to pursue this goal by a

A {Ti6W4}-Cluster-Substituted Polyoxotungstate: Synthesis, Structure, and Catalytic Oxidation Properties

A novel Ti-W-O-cluster-substituted tungstoantimonate (TA), [H2N(CH3)2]3Na4H9[{Ti6W4O18(OH)(H2O)3}(B-α-SbW9O33)3]·20H2O (1), has been made by hydrothermal reactions of trivacant [B-α-SbW9O33]9- units, Ti4+ cations, and WO42- anions in the presence of [H2N(CH3)2]·Cl and structurally characterized. Intriguingly, the polyoxoanion of 1 is constructed from three [B-α-SbW9O33]9- units and a previously unobserved decanuclear heterometallic Ti-W-O cluster [Ti6W4O18(OH)(H2O)3]11+ ({Ti6W4}) that is comprised of an octahedral [Ti6WO6(H2O)3]18+ cluster and an edge-sharing [W3O12(OH)]7- fragment via six W-O-Ti/W linkers. Furthermore, studies on the catalytic oxidation properties reveal that 1 possesses good catalytic activity toward the oxidation reactions of various sulfides and cyclooctene based on the environmentally friendly oxidant H2O2.