Search
Element Search
Structure Search
Thermo Scientific Chemicals
2-(Methylthio)naphthalene, 98%
CAS: 7433-79-6 | C11H10S | 174.261 g/mol
Have Questions?
Change view
Catalog number B22368.06
also known as B22368-06
Price (USD)
420.65
Online Exclusive
467.00Save 46.35 (10%)
Each
Quantity:
5 g
Price (USD)
420.65
Online Exclusive
467.00Save 46.35 (10%)
Each
Chemical Identifiers
CAS7433-79-6
IUPAC Name2-(methylsulfanyl)naphthalene
Molecular FormulaC11H10S
InChI KeySSKUUDUKJMIOKQ-UHFFFAOYSA-N
SMILESCSC1=CC=C2C=CC=CC2=C1
View more
Specifications
Specification Sheet
Specification SheetAppearance (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.
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.