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CAS

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83467-04-3

1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83467-04-3 Structure

  • Basic information

    1. Product Name: 1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine
    2. Synonyms:
    3. CAS NO:83467-04-3
    4. Molecular Formula:
    5. Molecular Weight: 246.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83467-04-3.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: 1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine(83467-04-3)
    11. EPA Substance Registry System: 1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine(83467-04-3)

  • 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: 83467-04-3(Hazardous Substances Data)

83467-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83467-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83467-04:
(7*8)+(6*3)+(5*4)+(4*6)+(3*7)+(2*0)+(1*4)=143
143 % 10 = 3
So 83467-04-3 is a valid CAS Registry Number.

83467-04-3Downstream Products

83467-04-3Relevant articles and documents

SYNTHESIS OF 1,1-DIAMINO-2-THIOACYLETHYLENES: A NOVEL C-THIOACYLATION BY THE WILLGERODT-KINDLER REACTION

Rajappa, S.,Nair, M. D.,Sreenivasan, R.,Advani, B. G.

, p. 1673 - 1676 (1982)

A novel C-thioacylation reaction is described.Reaction of aromatic or heterocyclic aldehydes with 1-alkyl-2-methyl-1,4,5,6-tetrahydropyrimidine or 1-alkyl-2-methylimidazolidine in the presence of sulphur leads to the thioacylketeneaminals 6,10 or 12 in low to moderate yields.The structure of 6e was proved by S-methylation to 7e and acid-hydrolysis to the known 8e.Oxidative cyclization of 6 leads to the isothiazolo(2,3-a) pyrimidinium salts 13.

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