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462110-58-3

3,5-Thiomorpholinedione,4-ethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 462110-58-3 Structure

  • Basic information

    1. Product Name: 3,5-Thiomorpholinedione,4-ethyl-(9CI)
    2. Synonyms: 3,5-Thiomorpholinedione,4-ethyl-(9CI)
    3. CAS NO:462110-58-3
    4. Molecular Formula: C6H9NO2S
    5. Molecular Weight: 159.20616
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 462110-58-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-Thiomorpholinedione,4-ethyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-Thiomorpholinedione,4-ethyl-(9CI)(462110-58-3)
    11. EPA Substance Registry System: 3,5-Thiomorpholinedione,4-ethyl-(9CI)(462110-58-3)

  • 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: 462110-58-3(Hazardous Substances Data)

462110-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 462110-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,2,1,1 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 462110-58:
(8*4)+(7*6)+(6*2)+(5*1)+(4*1)+(3*0)+(2*5)+(1*8)=113
113 % 10 = 3
So 462110-58-3 is a valid CAS Registry Number.

462110-58-3Downstream Products

462110-58-3Relevant articles and documents

Synthesis and pyrolysis of tetrahydro-1,4-oxazine-3,5-diones and tetrahydro-1,4-thiazine-3,5-diones

Aitken,Farrell,Kirton

, p. 1526 - 1531 (2007/10/03)

The preparation and characterization of six 4-substituted tetrahydro-l,4-oxazine-3,5-diones and five 4-substituted tetrahydro-l,4-thiazine-3,5-diones is described. Upon flash vacuum pyrolysis at 700°C these give N-substituted acetamides and nitriles, and a mechanism for formation of these products is proposed.

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