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N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132593-36-3 Structure
  • Basic information

    1. Product Name: N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide
    2. Synonyms: N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide
    3. CAS NO:132593-36-3
    4. Molecular Formula: C18H15N5O5S
    5. Molecular Weight: 413.4072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132593-36-3.mol
  • Chemical Properties

    1. Melting Point: 270-272 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.519±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 6.54±0.10(Predicted)
    10. CAS DataBase Reference: N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide(132593-36-3)
    12. EPA Substance Registry System: N-{4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl}-4-nitrobenzamide(132593-36-3)
  • 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: 132593-36-3(Hazardous Substances Data)

132593-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132593-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,9 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132593-36:
(8*1)+(7*3)+(6*2)+(5*5)+(4*9)+(3*3)+(2*3)+(1*6)=123
123 % 10 = 3
So 132593-36-3 is a valid CAS Registry Number.

132593-36-3Downstream Products

132593-36-3Relevant articles and documents

Synthesis of novel sulfonamide analogs containing sulfamerazine/sulfaguanidine and their biological activities

Aday, Burak,Sola, P?nar,?olak, Ferda?,Kaya, Muharrem

, p. 1005 - 1010 (2016)

Sulfamerazine and sulfaguanidine are clenched with p-nitrobenzoyl chloride and the products obtained are reduced to NaxS in ethanol–water. Novel sulfonamides (6a–g and 9a–g) were synthesized by the reaction of these reduced products (4 and 8) w

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