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CAS

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93322-81-7

Naphthalene, 2-methyl-1-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93322-81-7 Structure

  • Basic information

    1. Product Name: Naphthalene, 2-methyl-1-(phenylthio)-
    2. Synonyms:
    3. CAS NO:93322-81-7
    4. Molecular Formula: C17H14S
    5. Molecular Weight: 250.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93322-81-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Naphthalene, 2-methyl-1-(phenylthio)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Naphthalene, 2-methyl-1-(phenylthio)-(93322-81-7)
    11. EPA Substance Registry System: Naphthalene, 2-methyl-1-(phenylthio)-(93322-81-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93322-81-7(Hazardous Substances Data)

93322-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93322-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93322-81:
(7*9)+(6*3)+(5*3)+(4*2)+(3*2)+(2*8)+(1*1)=127
127 % 10 = 7
So 93322-81-7 is a valid CAS Registry Number.

93322-81-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-phenylsulfanylnaphthalene

1.2 Other means of identification

Product number -
Other names 2-methyl-1-phenylsulfonylnaphthalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:93322-81-7 SDS

93322-81-7Relevant articles and documents

Atropoisomerism in Hindered Naphthyl Sulfoxides: Structure, Stereodynamics, and Chiral Resolution

Casarini, D.,Foresti, E.,Gasparrini, F.,Lunazzi, L.,Macciantelli, D.,et al.

, p. 5674 - 5682 (1993)

Barriers for the E,Z interconversion of atropisomers of 1-naphthyl sulfoxides (ArSOR) having a methyl group at position 2 of the naphthalene moiety were measured by variable-temperature NMR.Their values were found to cover the range 10.6-18.4 kcal molsup

Carbon-sulfur bond formation catalyzed by [Pd(IPr*OMe) (cin)Cl] (cin = cinnamyl)

Bastug, Gulluzar,Nolan, Steven P.

supporting information, p. 9303 - 9308 (2013/10/08)

The newly prepared complex [Pd(IPr*OMe)(cin)(Cl)] provides high catalytic activity for carbon-sulfur cross-coupling reactions. Nonactivated and deactivated aryl halides were successfully coupled with a large variety of aryl- and alkylthiols using this well-defined palladium N-heterocyclic carbene (NHC) complex.

Fragmentation of anion radicals with elimination of aryloxy groups

Dneprovskii,Fedosov

, p. 1438 - 1443 (2007/10/03)

4-Vinylbenzyl phenyl ether, 4-phenylbenzyl phenyl ether, 1- and 2-naphthylmethyl phenyl ethers react with sodium thiophenolate under photochemical stimulation with replacement of the phenoxy group. The composition of reaction products and relation of reactivity to the structure of substrates is consistent with anion-radical mechanism. The corresponding methoxy and cyano derivatives do not undergo the reaction.

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