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133810-16-9

2-Methylsulfanyl-2-phenyl-1-p-tolyl-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133810-16-9 Structure

  • Basic information

    1. Product Name: 2-Methylsulfanyl-2-phenyl-1-p-tolyl-ethanol
    2. Synonyms:
    3. CAS NO:133810-16-9
    4. Molecular Formula:
    5. Molecular Weight: 258.384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133810-16-9.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: 2-Methylsulfanyl-2-phenyl-1-p-tolyl-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methylsulfanyl-2-phenyl-1-p-tolyl-ethanol(133810-16-9)
    11. EPA Substance Registry System: 2-Methylsulfanyl-2-phenyl-1-p-tolyl-ethanol(133810-16-9)

  • 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: 133810-16-9(Hazardous Substances Data)

133810-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133810-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,1 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133810-16:
(8*1)+(7*3)+(6*3)+(5*8)+(4*1)+(3*0)+(2*1)+(1*6)=99
99 % 10 = 9
So 133810-16-9 is a valid CAS Registry Number.

133810-16-9Downstream Products

133810-16-9Relevant articles and documents

SYNTHETIC USEFULNESS OF SILYL THIOKETONES: FUNCTIONALIZATION OF THEIR PRIMARY ADDUCTS THROUGH DESILYLATION AND TRAPPING BY CARBON ELECTROPHILES.

Bonini, Bianca F.,Masiero, Stefano,Mazzanti, Germana,Zani, Paolo

, p. 815 - 818 (1991)

Desilylation of either α-silyl sulphides or silyl dihydrothiopyrans (easily obtained from silyl thiones as primary adducts), when performed in the presence of carbon electrophiles (aldehydes or ketones), offers an easy entry to carbofunctionalised products.

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