2-(Methylthio)naphthalene, 98%

Name: 2-(Methylthio)naphthalene, 98%
SKU: B22368.06

CAS: 7433-79-6 | C11H10S | 174.261 g/mol

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Catalog number B22368.06

also known as B22368-06

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Chemical Identifiers

CAS7433-79-6

IUPAC Name2-(methylsulfanyl)naphthalene

Molecular FormulaC11H10S

InChI KeySSKUUDUKJMIOKQ-UHFFFAOYSA-N

SMILESCSC1=CC=C2C=CC=CC2=C1

Specifications

Specification Sheet

Appearance (Color)White to cream or pale brown

FormPowder

Assay (GC)≥97.5%

Melting Point (clear melt)55.0-61.0?C

2-(Methylthio)naphthalene is used to produce 1-chloro-2-methylsulfanylnaphthalene. This reaction will need reagent CuCl2-Al2O3, and the menstruum benzene

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-(Methylthio)naphthalene is used to produce 1-chloro-2-methylsulfanylnaphthalene. This reaction will need reagent CuCl2-Al2O3, and the menstruum benzene

Solubility
Slightly soluble in water

Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.

RUO – Research Use Only

General References:

Arnold Zweig.; Arthur H. Maurer.; Bernard George Roberts. Oxidation, reduction, and electrochemiluminescence of donor-substituted polycyclic aromatic hydrocarbons. J. Org. Chem. 1967, 32, (5), 1322-1329.
Mohammad Aslam.; Kenneth G. Davenport.; Wayne F. Stansbury. Anhydrous hydrogen fluoride catalyzed Friedel-Crafts reactions of thioaromatic compounds. J. Org. Chem.1991, 56, (20), 5955-5958.