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84406-07-5

diphenylthioacetate de methyle is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84406-07-5 Structure

  • Basic information

    1. Product Name: diphenylthioacetate de methyle
    2. Synonyms: diphenylthioacetate de methyle
    3. CAS NO:84406-07-5
    4. Molecular Formula:
    5. Molecular Weight: 290.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84406-07-5.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: diphenylthioacetate de methyle(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenylthioacetate de methyle(84406-07-5)
    11. EPA Substance Registry System: diphenylthioacetate de methyle(84406-07-5)

  • 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: 84406-07-5(Hazardous Substances Data)

84406-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84406-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,0 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84406-07:
(7*8)+(6*4)+(5*4)+(4*0)+(3*6)+(2*0)+(1*7)=125
125 % 10 = 5
So 84406-07-5 is a valid CAS Registry Number.

84406-07-5Relevant articles and documents

ORGANIC SYNTHESIS WITH α-CHLOROSULFIDES. CONVENIENT ROUTES TO PHENYLTHIOACETALS FROM α-DIAZOKETONES AND ALKYL PHENYL SULPHIDES VIA α-CHLOROSULPHIDES

Cronin, John P.,Dilworth, Bird M.,McKervey, M. Anthony

, p. 757 - 760 (2007/10/02)

α-Chloroalkyl phenyl sulphides, derived from either the action of benzenesulphenyl chloride on α-diazoketones or of N-chlorosuccinimide on alkyl phenyl sulphides, are converted into phenylthioacetals on exposure to thiophenol in the presence of zinc chloride.

α,α'-Bisphenylthiocarbonyles en synthese organique; applications en serie indolique

Massiot, Georges,Mulamba, Tshilundu,Levy, Jean

, p. 241 - 248 (2007/10/02)

α'α'-bisphenylthioesters have been prepared by a Michael reaction between methyl bisphenylthioacetate and unencumbered activated olefins.They have been transformed into monosulfenylated esters by thiophenol in the presence of a catalytic amount of base.Th

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