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18614-67-0

2-Methyl-5-nitropyridin-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18614-67-0 Structure

  • Basic information

    1. Product Name: 2-Methyl-5-nitropyridin-4-ol
    2. Synonyms: 2-Methyl-5-nitropyridin-4-ol
    3. CAS NO:18614-67-0
    4. Molecular Formula: C6H6N2O3
    5. Molecular Weight: 154.12344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18614-67-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Methyl-5-nitropyridin-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methyl-5-nitropyridin-4-ol(18614-67-0)
    11. EPA Substance Registry System: 2-Methyl-5-nitropyridin-4-ol(18614-67-0)

  • 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: 18614-67-0(Hazardous Substances Data)

18614-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18614-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18614-67:
(7*1)+(6*8)+(5*6)+(4*1)+(3*4)+(2*6)+(1*7)=120
120 % 10 = 0
So 18614-67-0 is a valid CAS Registry Number.

18614-67-0Downstream Products

18614-67-0Relevant articles and documents

ANTIBIOTIC COMPOUNDS

-

, (2018/03/25)

The present invention relates to antibiotic compounds of formula (I), to compositions containing these compounds and to methods of treating bacterial diseases and infections using the compounds. The compounds find application in the treatment of infection with, and diseases caused by, Gram-positive and/or Gram-negative bacteria, and in particular in the treatment of infection with, and diseases caused by, Neisseria gonorrhoeae.

A Unified Approach to the Isomeric α-, β-, γ-, and δ-Carbolines via their 6,7,8,9-Tetrahydro Counterparts

Yan, Qiao,Gin, Emma,Banwell, Martin G.,Willis, Anthony C.,Carr, Paul D.

, p. 4328 - 4335 (2017/04/28)

A cross-coupling/reductive cyclization protocol has been employed in a unified approach to all four carbolines. So, for example, the 2-nitropyridine 8, which is readily prepared through an efficient palladium-catalyzed Ullmann cross-coupling reaction, is reductively cyclized under conventional conditions to give 6,7,8,9-tetrahydro-α-carboline that is itself readily aromatized to give α-carboline (1).

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