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N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 602327-76-4 Structure
  • Basic information

    1. Product Name: N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide
    2. Synonyms: N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide
    3. CAS NO:602327-76-4
    4. Molecular Formula:
    5. Molecular Weight: 398.483
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 602327-76-4.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: N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide(602327-76-4)
    11. EPA Substance Registry System: N,N-diallyl-5-benzyl-1,3-dihydro-2,2,4-trioxo-5H-thieno[3,4-c]pyridin-3-carboxamide(602327-76-4)
  • 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: 602327-76-4(Hazardous Substances Data)

602327-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 602327-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,2,3,2 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 602327-76:
(8*6)+(7*0)+(6*2)+(5*3)+(4*2)+(3*7)+(2*7)+(1*6)=124
124 % 10 = 4
So 602327-76-4 is a valid CAS Registry Number.

602327-76-4Downstream Products

602327-76-4Relevant articles and documents

Diels-Alder reactions of pyridinone o-quinodimethanes generated from substituted sulfolene[3,4-c]pyridin-4(1H)-ones

Govaerts, Tom C.,Vogels, Ilse A.,Compernolle, Frans,Hoornaert, Georges J.

, p. 5481 - 5494 (2007/10/03)

1-Benzyl-3-(bromomethyl)-2(1H)-pyrazinone was converted to [3,4-c] sulfolene pyridinone 8a and further (1- or 3-) substituted derivatives having a dienophilic side chain on the sulfolene ring. Thermolytic extrusion of sulfur dioxide from o-QDM precursor 8

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