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933252-22-3

4-methyl-N-[4-(4-methylphenyl)-6-phenylpyrimidin-2-yl]benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 933252-22-3 Structure

  • Basic information

    1. Product Name: 4-methyl-N-[4-(4-methylphenyl)-6-phenylpyrimidin-2-yl]benzenesulfonamide
    2. Synonyms:
    3. CAS NO:933252-22-3
    4. Molecular Formula:
    5. Molecular Weight: 415.516
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 933252-22-3.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-methyl-N-[4-(4-methylphenyl)-6-phenylpyrimidin-2-yl]benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-N-[4-(4-methylphenyl)-6-phenylpyrimidin-2-yl]benzenesulfonamide(933252-22-3)
    11. EPA Substance Registry System: 4-methyl-N-[4-(4-methylphenyl)-6-phenylpyrimidin-2-yl]benzenesulfonamide(933252-22-3)

  • 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: 933252-22-3(Hazardous Substances Data)

933252-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 933252-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,2,5 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 933252-22:
(8*9)+(7*3)+(6*3)+(5*2)+(4*5)+(3*2)+(2*2)+(1*2)=153
153 % 10 = 3
So 933252-22-3 is a valid CAS Registry Number.

933252-22-3Downstream Products

933252-22-3Relevant articles and documents

Tailored-design Synthesis of Sulfapyrimidine Derivatives

Azzam, Rasha A.

, p. 619 - 627 (2019)

In this paper, we report an efficient and convenient approach for the synthesis of tailored-design target sulfapyrimidine derivatives expected to show remarkable antimicrobial activities. The approach is based on reacting arylsulfonyl guanidine with α,β-unsaturated carbonyl compounds to afford N-(4,6-diarylpyrimidin-2-yl)arylsulfonamide or with ylidene derivatives to afford N-(6-aryl-5-cyanopyrimidin-2-yl)arylsulfonamide, N-(4-amino-5-cyano-6-(methylthio)-pyrimidin-2-yl)-arylsulfonamide, and N-(5-cyanopyrimidin-2-yl)arylsulfonamide compounds through Michael addition reaction. The structure of the newly synthesized compounds was confirmed from spectral data and elemental analysis.

Synthesis, characterization, and anti-amoebic activity of N-(pyrimidin-2-yl)benzenesulfonamide derivatives

Roouf Bhat, Abdul,Arshad, Mohammad,Ju Lee, Eun,Pokharel, Smritee,Choi, Inho,Athar, Fareeda

, p. 2267 - 2277 (2014/01/06)

A new series of N-(pyrimidin-2-yl)benzenesulfonamide derivatives, 3a-3i and 4a-4i, was synthesized from pyrimidin-2-amines, 2a-2i, with the aim to explore their effects on in vitro growth of Entamoeba histolytica. The chemical structures of the compounds

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