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268536-10-3

6-anisyl-1,3-dioxine-4-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 268536-10-3 Structure

  • Basic information

    1. Product Name: 6-anisyl-1,3-dioxine-4-thione
    2. Synonyms: 6-anisyl-1,3-dioxine-4-thione
    3. CAS NO:268536-10-3
    4. Molecular Formula:
    5. Molecular Weight: 250.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 268536-10-3.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: 6-anisyl-1,3-dioxine-4-thione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-anisyl-1,3-dioxine-4-thione(268536-10-3)
    11. EPA Substance Registry System: 6-anisyl-1,3-dioxine-4-thione(268536-10-3)

  • 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: 268536-10-3(Hazardous Substances Data)

268536-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 268536-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,8,5,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 268536-10:
(8*2)+(7*6)+(6*8)+(5*5)+(4*3)+(3*6)+(2*1)+(1*0)=163
163 % 10 = 3
So 268536-10-3 is a valid CAS Registry Number.

268536-10-3Downstream Products

268536-10-3Relevant articles and documents

Acylthioketene-Thioacylketene-Thiet-2-one Rearrangements

Ammann, Jeffrey R.,Flammang, Robert,Wong, Ming Wah,Wentrup, Curt

, p. 2706 - 2710 (2000)

Flash vacuum thermolysis (FVT) of 6-aryl-1,3-dioxine-4-thiones 9 leads to the formation of acylthioketenes 10, which are characterized by Ar matrix IR spectroscopy as well as on-line tandem mass spectrometry. The thioketenes 10 undergo a 1,3-shift of the aryl group to generate thioacylketenes 11. Ketenes 11 cyclize to 3-aryl-thiet-2-ones 12, which are also characterized by matrix IR spectroscopy and tandem mass spectrometry. The thiet-2-ones 12 undergo two kinds of reaction under the FVT conditions: (i) cheletropic CO extrusion with formation of arylthioketenes 13, and (ii) cycloreversion to COS and arylacetylene.

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