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CAS

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24541-52-4

Pyrido[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24541-52-4 Structure

  • Basic information

    1. Product Name: Pyrido[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-phenyl-
    2. Synonyms:
    3. CAS NO:24541-52-4
    4. Molecular Formula: C13H9N3O2
    5. Molecular Weight: 239.233
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24541-52-4.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: Pyrido[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrido[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-phenyl-(24541-52-4)
    11. EPA Substance Registry System: Pyrido[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-phenyl-(24541-52-4)

  • 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: 24541-52-4(Hazardous Substances Data)

24541-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24541-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24541-52:
(7*2)+(6*4)+(5*5)+(4*4)+(3*1)+(2*5)+(1*2)=94
94 % 10 = 4
So 24541-52-4 is a valid CAS Registry Number.

24541-52-4Downstream Products

24541-52-4Relevant articles and documents

NOVEL SYNTHESIS OF PYRIDOPYRIMIDINE DIONES

Fahmy, Amin Farouk,Youssef, Mohamed Salah Kamel,Halim, Mohamed Said Abdel,Hassan, Mamdouh Adly,Sauer, Jourgin

, p. 2201 - 2213 (2007/10/02)

N-(Phenylsulphonyloxy)quinolinimide (I) reacts with different nucleophiles to give II-VIII.It was proved that the nucleophilic attack occurs at the more electro-positive carbonyl group to give only one product in good yields.

Heteroacyl Azides as Acylating Agents for Aromatic or Heteroatomic Amines (1)

Stanovnik, B.,Tisler, M.,Golob, V.,Hvala, I.,Nikolic, O.

, p. 733 - 736 (2007/10/02)

The possibility of formation of substituted heterocyclic amides from heteroacyl azides and aromatic or heteroatomic amines was investigated.Although acylation proceeded in some cases under mild reaction conditions, formation of N,N'-disubstituted ureas was the main process at elevated temperatures.

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