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4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 283168-85-4 Structure
  • Basic information

    1. Product Name: 4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)-
    2. Synonyms: 4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)-
    3. CAS NO:283168-85-4
    4. Molecular Formula: C7H8N2O2S
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 283168-85-4.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: 4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)-(283168-85-4)
    11. EPA Substance Registry System: 4(3H)-Pyrimidinone, 3-acetyl-2-(methylthio)-(283168-85-4)
  • 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: 283168-85-4(Hazardous Substances Data)

283168-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 283168-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,3,1,6 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 283168-85:
(8*2)+(7*8)+(6*3)+(5*1)+(4*6)+(3*8)+(2*8)+(1*5)=164
164 % 10 = 4
So 283168-85-4 is a valid CAS Registry Number.

283168-85-4Downstream Products

283168-85-4Relevant articles and documents

Synthesis of nitrogen bicyclic scaffolds: Pyrimido[1,2-a]pyrimidine-2,6- diones

Grosjean, Sylvain,Triki, Smail,Meslin, Jean-Claude,Julienne, Karine,Deniaud, David

scheme or table, p. 9912 - 9924 (2011/02/22)

The multi-step synthesis of 1,3,7-trisubstituted pyrimido[1,2-a] pyrimidinediones starting from isothiocyanates is described. These nitrogen bicycles were prepared by an iterative sequence of functionalization/ cyclocondensation reactions. [4+2] Cycloaddition reactions took place between diazadienic chains and various acyl chlorides providing sophisticated heterobicycles.

New 1,3-diazadienes used in heterocyclic synthesis

Friot, Celine,Reliquet, Alain,Reliquet, Francoise,Meslin, Jean Claude

, p. 695 - 702 (2007/10/03)

The synthesis of dihydropyrimidines, dihydropyrimidinones and thiadiazine-1,1-dioxides starting from neutral or cationic 2-methylthio-1,3- diazadienes is described. Addition of H2S followed by loss of methanethiol led to the corresponding thiocarbonyl compounds.

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