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CAS

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138415-70-0

4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)

    Cas No: 138415-70-0

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  • 138415-70-0 Structure

  • Basic information

    1. Product Name: 4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)
    2. Synonyms: 4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)
    3. CAS NO:138415-70-0
    4. Molecular Formula: C8H15N3O4
    5. Molecular Weight: 217.2224
    6. EINECS: N/A
    7. Product Categories: ETHOXY
    8. Mol File: 138415-70-0.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(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)(138415-70-0)
    11. EPA Substance Registry System: 4(1H)-Pyrimidinone,2-amino-5,6-diethoxy-5,6-dihydro-5-hydroxy-(9CI)(138415-70-0)

  • 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: 138415-70-0(Hazardous Substances Data)

138415-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138415-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138415-70:
(8*1)+(7*3)+(6*8)+(5*4)+(4*1)+(3*5)+(2*7)+(1*0)=130
130 % 10 = 0
So 138415-70-0 is a valid CAS Registry Number.

138415-70-0Downstream Products

138415-70-0Relevant articles and documents

A Versatile and Convenient Method for the Syntheses of Pyrimidothiazine and -thiazepine Ring Systems

Sako, Magoichi,Totani, Reiko,Konohara, Minako,Hirota, Kosaku,Maki, Yoshifumi

, p. 2675 - 2677 (2007/10/02)

Treatment of 5-hydroxyuracil 1 and 5-hydroxyisocytosine 2 with N-bromosuccinimide in ethanol followed by the thermal condensation with β- and γ-amino thiols such as 2-aminothiophenol, cysteamine, L-cysteine and D,L-homocysteine resulted in the formation of the corresponding pyrimidothiazin-4(3H)-ones, 3-8, and pyrimidothiazine and -thiazepine ring systems was shown to involve the condensation of 5,6-diethoxy-5-hydroxy-5,6-dihydropyrimidin-4(3H)-one intermediates, 11 and 12, with the β- and γ-amino thiols which is accelerated in the presence of an acid-catalyst.

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