35330-76-8

Basic information

• Product Name: 2-(Methylsulfinyl)naphthalene ,97%
• Synonyms: 2-(Methylsulfinyl)naphthalene ,97%
• CAS NO: 35330-76-8
• Molecular Formula: C₁₁H₁₀OS
• Molecular Weight: 190
• Mol File: 35330-76-8.mol
• Article Data: 90

Chemical Properties

• Boiling Point: 384.2°C at 760 mmHg
• Flash Point: 186.2°C
• Appearance: /
• Density: 1.25g/cm³
• Vapor Pressure: 9.17E-06mmHg at 25°C
• Refractive Index: 1.69
• CAS DataBase Reference: 2-(Methylsulfinyl)naphthalene ,97%(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(Methylsulfinyl)naphthalene ,97%(35330-76-8)
• EPA Substance Registry System: 2-(Methylsulfinyl)naphthalene ,97%(35330-76-8)

Safety Data

• Statements: 22-34
• Safety Statements: 26-36/37/39-35
• Hazardous Substances Data: 35330-76-8(Hazardous Substances Data)

Usage

Chemical Properties

Off-white solid

InChI:InChI=1/C11H10OS/c1-13(12)11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3

Upstream product

• 7433-79-6 2-methylthionaphthalene 
• 60142-34-9 2-Bromomethanesulfinyl-naphthalene 
• 105163-67-5 4-[2-(Naphthalene-2-sulfinyl)-ethyl]-pyridine 
• 74-88-4 methyl iodide 
• 138286-19-8 (+)-(Z)-2-(2-bromoethenylsulfinyl)naphthalene 
• 35330-76-8 (R)-2-naphthyl methyl sulfoxide 
• 134613-51-7 (Z)-2-(2-bromoethenylthio)naphthalene 
• 105163-70-0 2-naphthyl 2-(4-pyridyl)ethyl sulfide 
• 91-60-1 2-Naphthalenethiol 
• 67-68-5 dimethyl sulfoxide 
• 75-16-1 methylmagnesium bromide 
• 1308834-02-7 2-(2-naphthylsulfanyl)ethyl phenyl sulfone 
• 1308833-67-1 2-(naphthylsulfinyl)ethyl phenyl sulfone 

Downstream Products

• 35330-75-7 2-(methylsulfonyl)naphthalene 
• 38306-18-2 5-(Naphthalene-2-sulfinylmethyl)-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol 
• 38306-17-1 9-(Naphthalene-2-sulfinylmethyl)-9H-fluoren-9-ol 
• 38226-53-8 1-(Naphthalene-2-sulfinylmethyl)-cyclohexanol 
• 38226-61-8 C₂₆H₂₂O₂S 
• 38226-50-5 1-(4-Dimethylamino-phenyl)-2-(naphthalene-2-sulfinyl)-ethanol 
• 38226-63-0 C₂₇H₂₄O₃S 
• 38226-51-6 2-(4-Methoxy-phenyl)-1-(naphthalene-2-sulfinyl)-propan-2-ol 
• 38226-62-9 C₂₇H₂₄O₂S 
• 38226-60-7 [2-(Naphthalene-2-sulfinyl)-1-phenyl-ethyl]-phenyl-amine 
• 38226-52-7 1-(Naphthalene-2-sulfinyl)-2-phenyl-pentan-2-ol 
• 38306-16-0 4-(Naphthalene-2-sulfinyl)-2,3-diphenyl-butyronitrile 
• 35330-76-8 (R)-2-naphthyl methyl sulfoxide 
• 114129-50-9 (S)-methyl 2-naphthylsulfoxide 

Relevant articles and documents

2D and 3D Porphyrinic Covalent Organic Frameworks: The Influence of Dimensionality on Functionality

The construction of 2D and 3D covalent organic frameworks (COFs) from functional moieties for desired properties has gained much attention. However, the influence of COFs dimensionality on their functionalities, which can further assist in COF design, has

Ligand Modification of Au25 Nanoclusters for Near-Infrared Photocatalytic Oxidative Functionalization

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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.