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CAS

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355152-21-5

N-(4,6-dimethylpyrimidin-2-yl)-4-[(1H-indol-3-ylmethylene)amino]benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 355152-21-5 Structure

  • Basic information

    1. Product Name: N-(4,6-dimethylpyrimidin-2-yl)-4-[(1H-indol-3-ylmethylene)amino]benzenesulfonamide
    2. Synonyms:
    3. CAS NO:355152-21-5
    4. Molecular Formula:
    5. Molecular Weight: 405.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 355152-21-5.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: N-(4,6-dimethylpyrimidin-2-yl)-4-[(1H-indol-3-ylmethylene)amino]benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4,6-dimethylpyrimidin-2-yl)-4-[(1H-indol-3-ylmethylene)amino]benzenesulfonamide(355152-21-5)
    11. EPA Substance Registry System: N-(4,6-dimethylpyrimidin-2-yl)-4-[(1H-indol-3-ylmethylene)amino]benzenesulfonamide(355152-21-5)

  • 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: 355152-21-5(Hazardous Substances Data)

355152-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355152-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,1,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 355152-21:
(8*3)+(7*5)+(6*5)+(5*1)+(4*5)+(3*2)+(2*2)+(1*1)=125
125 % 10 = 5
So 355152-21-5 is a valid CAS Registry Number.

355152-21-5Downstream Products

355152-21-5Relevant articles and documents

Identification of antibacterial and antifungal pharmacophore sites for potent bacteria and fungi inhibition: Indolenyl sulfonamide derivatives

Chohan, Zahid H.,Youssoufi, Moulay H.,Jarrahpour, Aliasghar,Ben Hadda, Taibi

, p. 1189 - 1199 (2010)

Synthesis of seven new indolenyl sulfonamides, have been prepared by the condensation reaction of indole-3-carboxaldehyde with different sulfonamides such as, sulphanilamide, sulfaguanidine, sulfathiazole, sulfamethoxazole, sulfisoxazole, sulfadiazine and

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