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100947-02-2

4-methyl-6-(2-phenylethyl)tetrahydro-2H-thiopyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100947-02-2 Structure

  • Basic information

    1. Product Name: 4-methyl-6-(2-phenylethyl)tetrahydro-2H-thiopyran-2-one
    2. Synonyms:
    3. CAS NO:100947-02-2
    4. Molecular Formula:
    5. Molecular Weight: 232.346
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100947-02-2.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: 4-methyl-6-(2-phenylethyl)tetrahydro-2H-thiopyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-6-(2-phenylethyl)tetrahydro-2H-thiopyran-2-one(100947-02-2)
    11. EPA Substance Registry System: 4-methyl-6-(2-phenylethyl)tetrahydro-2H-thiopyran-2-one(100947-02-2)

  • 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: 100947-02-2(Hazardous Substances Data)

100947-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100947-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,4 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100947-02:
(8*1)+(7*0)+(6*0)+(5*9)+(4*4)+(3*7)+(2*0)+(1*2)=92
92 % 10 = 2
So 100947-02-2 is a valid CAS Registry Number.

100947-02-2Downstream Products

100947-02-2Relevant articles and documents

Thioaldehyde Diels-Alder Reactions

Vedejs, E.,Eberlein, T. H.,Mazur, D. J.,McClure, C. K.,Perry, D. A.,et al.

, p. 1556 - 1562 (2007/10/02)

Thioaldehydes containing virtually any α-substitutent can be generated by photofragmentation of phenacyl sulfides.Donor-substituted derivatives are reactive toward electron-rich dienes and give 2 + 4 cycloadducts with regiochemistry corresponding to advan

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