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1372893-09-8

C25H26N6O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1372893-09-8 Structure

  • Basic information

    1. Product Name: C25H26N6O4
    2. Synonyms:
    3. CAS NO:1372893-09-8
    4. Molecular Formula:
    5. Molecular Weight: 474.519
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1372893-09-8.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: C25H26N6O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C25H26N6O4(1372893-09-8)
    11. EPA Substance Registry System: C25H26N6O4(1372893-09-8)

  • 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: 1372893-09-8(Hazardous Substances Data)

1372893-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372893-09-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,8,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1372893-09:
(9*1)+(8*3)+(7*7)+(6*2)+(5*8)+(4*9)+(3*3)+(2*0)+(1*9)=188
188 % 10 = 8
So 1372893-09-8 is a valid CAS Registry Number.

1372893-09-8Downstream Products

1372893-09-8Relevant articles and documents

New oxadiazole derivatives of isonicotinohydrazide in the search for antimicrobial agents: Synthesis and in vitro evaluation

Malhotra, Manav,Sanduja, Mohit,Samad, Abdul,Deep, Aakash

, p. 9 - 16 (2012)

Structural modifications of the front line antitubercular drug isoniazid provide lipophilic adaptations of the drug in which the hydrazide moiety of isoniazid is replaced by 1,3,4-oxadiazole heterocycles to eliminate in vivo acetylation by arylamine N-ace

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