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N-(1H-benzoimidazol-2-yl)-3,5-dinitro-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73648-57-4 Structure
  • Basic information

    1. Product Name: N-(1H-benzoimidazol-2-yl)-3,5-dinitro-benzamide
    2. Synonyms:
    3. CAS NO:73648-57-4
    4. Molecular Formula:
    5. Molecular Weight: 327.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73648-57-4.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: N-(1H-benzoimidazol-2-yl)-3,5-dinitro-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1H-benzoimidazol-2-yl)-3,5-dinitro-benzamide(73648-57-4)
    11. EPA Substance Registry System: N-(1H-benzoimidazol-2-yl)-3,5-dinitro-benzamide(73648-57-4)
  • 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: 73648-57-4(Hazardous Substances Data)

73648-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73648-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,4 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73648-57:
(7*7)+(6*3)+(5*6)+(4*4)+(3*8)+(2*5)+(1*7)=154
154 % 10 = 4
So 73648-57-4 is a valid CAS Registry Number.

73648-57-4Downstream Products

73648-57-4Relevant articles and documents

13C NMR spectra and biological activity of N-(1H-benzimidazol-2- yl)benzamides

Pilyugin,Sapozhnikov,Davydov,Chikisheva,Vorob'eva,Klimakova,Kiseleva,Kuznetsova,Davletov,Sapozhnikova,Yumadilov

, p. 1653 - 1659 (2006)

Derivatives of 1H-benzimidazol-2-amine and halo-, nitro-, methoxy-, and hydroxy-substituted benzoic acids were synthesized, and their fungicide activity against pure Fusarium culmorum and Helminthosporium sativum cultures and pathogenic microflora of wheat and barley seeds in laboratory and field tests was studied. Some compounds were found to exhibit a strong fungicide activity. Nauka/Interperiodica 2006.

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