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CAS

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86211-08-7

S-methyl nonanethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86211-08-7 Structure

  • Basic information

    1. Product Name: S-methyl nonanethioate
    2. Synonyms: S-methyl nonanethioate
    3. CAS NO:86211-08-7
    4. Molecular Formula:
    5. Molecular Weight: 188.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86211-08-7.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: S-methyl nonanethioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-methyl nonanethioate(86211-08-7)
    11. EPA Substance Registry System: S-methyl nonanethioate(86211-08-7)

  • 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: 86211-08-7(Hazardous Substances Data)

86211-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86211-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,1 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86211-08:
(7*8)+(6*6)+(5*2)+(4*1)+(3*1)+(2*0)+(1*8)=117
117 % 10 = 7
So 86211-08-7 is a valid CAS Registry Number.

86211-08-7Relevant articles and documents

Rhodium-catalyzed acyl-transfer reaction between benzyl ketones and thioesters: Synthesis of unsymmetric ketones by ketone CO-C bond cleavage and intermolecular rearrangement

Arisawa, Mieko,Kuwajima, Manabu,Toriyama, Fumihiko,Li, Guangzhe,Yamaguchi, Masahiko

supporting information; experimental part, p. 3804 - 3807 (2012/09/07)

In the presence of catalytic amounts of RhH(CO)(PPh3) 3 and 1,2-bis(diphenylphosphino)benzene (dppBz), acyl groups were transferred between benzyl ketones and thioesters/aryl esters. The rhodium complex catalyzed the cleavage of keto

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