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1316315-11-3

C15H15N3O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1316315-11-3 Structure

  • Basic information

    1. Product Name: C15H15N3O3
    2. Synonyms:
    3. CAS NO:1316315-11-3
    4. Molecular Formula:
    5. Molecular Weight: 285.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1316315-11-3.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: C15H15N3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H15N3O3(1316315-11-3)
    11. EPA Substance Registry System: C15H15N3O3(1316315-11-3)

  • 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: 1316315-11-3(Hazardous Substances Data)

1316315-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1316315-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,3,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1316315-11:
(9*1)+(8*3)+(7*1)+(6*6)+(5*3)+(4*1)+(3*5)+(2*1)+(1*1)=113
113 % 10 = 3
So 1316315-11-3 is a valid CAS Registry Number.

1316315-11-3Downstream Products

1316315-11-3Relevant articles and documents

Isonicotinic acid hydrazide derivatives: Synthesis, antimicrobial activity, and QSAR studies

Judge, Vikramjeet,Narasimhan, Balasubramanian,Ahuja, Munish,Sriram, Dharmarajan,Yogeeswari, Perumal,De Clercq, Erik,Pannecouque, Christophe,Balzarini, Jan

, p. 1451 - 1470 (2012)

A series of isonicotinic acid hydrazide derivatives (1-19) was synthesized and tested in vitro for antimycobacterial activity against Mycobacterium tuberculosis and antimicrobial activity against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Candida albicans, and Aspergillus niger and the results indicated that the compounds with OH, SCH3, and OCH 3 groups were found to be active against the tested strains. None of the test compounds were active against a broad variety of RNA and DNA viruses at subtoxic concentrations, except 8, that showed some selective anti-reovirus-1 activity. The multi-target QSAR models were found to be effective in predicting the antimicrobial activity of the isoniazid derivatives and indicated the importance of nuclear repulsion energy (Nu.E) in explaining the antimicrobial activity of isoniazid derivatives. The developed QSAR models were validated using the external test set of synthesized derivatives. Springer Science+Business Media, LLC 2011.

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