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CAS

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212574-12-4

Acetic acid 2-(3,5-dioxo-6-phenylsulfanyl-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethoxy)-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 212574-12-4 Structure

  • Basic information

    1. Product Name: Acetic acid 2-(3,5-dioxo-6-phenylsulfanyl-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethoxy)-ethyl ester
    2. Synonyms:
    3. CAS NO:212574-12-4
    4. Molecular Formula:
    5. Molecular Weight: 337.356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 212574-12-4.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: Acetic acid 2-(3,5-dioxo-6-phenylsulfanyl-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethoxy)-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid 2-(3,5-dioxo-6-phenylsulfanyl-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethoxy)-ethyl ester(212574-12-4)
    11. EPA Substance Registry System: Acetic acid 2-(3,5-dioxo-6-phenylsulfanyl-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethoxy)-ethyl ester(212574-12-4)

  • 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: 212574-12-4(Hazardous Substances Data)

212574-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212574-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,5,7 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 212574-12:
(8*2)+(7*1)+(6*2)+(5*5)+(4*7)+(3*4)+(2*1)+(1*2)=104
104 % 10 = 4
So 212574-12-4 is a valid CAS Registry Number.

212574-12-4Downstream Products

212574-12-4Relevant articles and documents

As-triazine derivatives with potential therapeutic action. XXVI.1 Synthesis of 5-substituted-6-azauracil acyclonucleosides

Cristescu, Carol,Czobor, Francisc

, p. 1319 - 1324 (1998)

5-Substituted 6-azauracils were alkylated with (2-acetoxyethoxy)methyl bromide to give protected acyclic nucleosides which were deprotected to afford acyclonucleosides of 5-substituted 6-azauracils. Their structures have been established by the UV and su

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