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CAS

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879499-34-0

2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 879499-34-0 Structure

  • Basic information

    1. Product Name: 2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol
    2. Synonyms: 2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol
    3. CAS NO:879499-34-0
    4. Molecular Formula:
    5. Molecular Weight: 301.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 879499-34-0.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: 2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol(879499-34-0)
    11. EPA Substance Registry System: 2-(4-isopropoxy-6-methyl-pyrimidin-2-ylamino)-3-phenyl-propan-1-ol(879499-34-0)

  • 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: 879499-34-0(Hazardous Substances Data)

879499-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879499-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,4,9 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 879499-34:
(8*8)+(7*7)+(6*9)+(5*4)+(4*9)+(3*9)+(2*3)+(1*4)=260
260 % 10 = 0
So 879499-34-0 is a valid CAS Registry Number.

879499-34-0Upstream product

879499-34-0Relevant articles and documents

A simple approach for the regioselective synthesis of imidazo[1,2-a] pyrimidiones and pyrimido[1,2-a]pyrimidinones

Font, David,Linden, Anthony,Heras, Montserrat,Villalgordo, José M.

, p. 1433 - 1443 (2006)

Several imidazo and pyrimido[1,2-a]pyrimidinones of type 1 and 2 were synthesized through intramolecular cyclization of pyrimidines 9 or pyrimidinones 10 bearing a variety of β and γ-aminoalcohols at the 2-position. Ring closure of the pyrimidinones of type 10 under Mitsunobu conditions lead to mixtures of both bicyclic regioisomers 1 and 2. Treatment of pyrimidines of type 9 with H2SO4 provided an efficient and operationally simple one-pot hydrolysis-cyclization procedure for obtaining imidazo and pyrimido[1,2-a]pyrimidinones 1 in good yields as the sole regioisomeric bicyclic product.

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