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CAS

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1579202-97-3

S-furfuryl 3-methoxybenzothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1579202-97-3 Structure

  • Basic information

    1. Product Name: S-furfuryl 3-methoxybenzothioate
    2. Synonyms:
    3. CAS NO:1579202-97-3
    4. Molecular Formula:
    5. Molecular Weight: 248.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1579202-97-3.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-furfuryl 3-methoxybenzothioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-furfuryl 3-methoxybenzothioate(1579202-97-3)
    11. EPA Substance Registry System: S-furfuryl 3-methoxybenzothioate(1579202-97-3)

  • 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: 1579202-97-3(Hazardous Substances Data)

1579202-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1579202-97-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,2,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1579202-97:
(9*1)+(8*5)+(7*7)+(6*9)+(5*2)+(4*0)+(3*2)+(2*9)+(1*7)=193
193 % 10 = 3
So 1579202-97-3 is a valid CAS Registry Number.

1579202-97-3Downstream Products

1579202-97-3Relevant articles and documents

Organocatalyzed anodic oxidation of aldehydes to thioesters

Ogawa, Kelli A.,Boydston, Andrew J.

, p. 1928 - 1931 (2014)

A method has been developed for the direct conversion of aldehydes to thioesters via integration of organocatalysis and electrosynthesis. The thiazolium precatalyst was found to facilitate oxidation of thiolate anions, leading to deleterious formation of disulfide byproducts. By circumventing this competing reaction, thioesters were obtained in good-to-excellent yields for a broad range of aldehyde and thiol substrates. This approach provides an atom-efficient thioesterification that circumvents the need for stoichiometric exogenous oxidants, high cell potentials, or redox mediators.

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