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CAS

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1158792-95-0

4-hydroxy-2-(isopropylamino)-6-phenylpyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1158792-95-0 Structure

  • Basic information

    1. Product Name: 4-hydroxy-2-(isopropylamino)-6-phenylpyrimidine
    2. Synonyms:
    3. CAS NO:1158792-95-0
    4. Molecular Formula:
    5. Molecular Weight: 229.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1158792-95-0.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: 4-hydroxy-2-(isopropylamino)-6-phenylpyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-hydroxy-2-(isopropylamino)-6-phenylpyrimidine(1158792-95-0)
    11. EPA Substance Registry System: 4-hydroxy-2-(isopropylamino)-6-phenylpyrimidine(1158792-95-0)

  • 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: 1158792-95-0(Hazardous Substances Data)

1158792-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158792-95-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,7,9 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1158792-95:
(9*1)+(8*1)+(7*5)+(6*8)+(5*7)+(4*9)+(3*2)+(2*9)+(1*5)=200
200 % 10 = 0
So 1158792-95-0 is a valid CAS Registry Number.

1158792-95-0Relevant articles and documents

Facile synthesis of 2,4-diamino-6-alkyl- or 6-aryl-pyrimidine derivatives

Wang, Xihong,Sathunuru, Ramadas,Melendez, Victor,Kozar, Michael P.,Lin, Ai J.

experimental part, p. 1056 - 1061 (2010/10/21)

(Chemical Equation Presented) Facile methods were developed to prepare a series of 6-phenyl and 6-alkyl-2,4-diaminopyrimidine derivatives. The pyrimidine ring of the final products was constructed by treatment of a 1,3-dicarbonyl derivative with an amidin

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