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CAS

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1263189-19-0

C18H13Cl2NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1263189-19-0 Structure

  • Basic information

    1. Product Name: C18H13Cl2NO3
    2. Synonyms:
    3. CAS NO:1263189-19-0
    4. Molecular Formula:
    5. Molecular Weight: 362.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1263189-19-0.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: C18H13Cl2NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H13Cl2NO3(1263189-19-0)
    11. EPA Substance Registry System: C18H13Cl2NO3(1263189-19-0)

  • 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: 1263189-19-0(Hazardous Substances Data)

1263189-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263189-19-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,1,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1263189-19:
(9*1)+(8*2)+(7*6)+(6*3)+(5*1)+(4*8)+(3*9)+(2*1)+(1*9)=160
160 % 10 = 0
So 1263189-19-0 is a valid CAS Registry Number.

1263189-19-0Downstream Products

1263189-19-0Relevant articles and documents

Discovery of a potent enoyl-acyl carrier protein reductase (FabI) inhibitor suitable for antistaphylococcal agent

Kim, Yun Gyeong,Seo, Jae Hong,Kwak, Jin Hwan,Shin, Kye Jung

, p. 4481 - 4486 (2015/10/12)

We report the discovery, synthesis, and biological activities of phenoxy-4-pyrone and phenoxy-4-pyridone derivatives as novel inhibitors of enoyl-acyl carrier protein reductase (FabI). Pyridone derivatives showed better activities than pyrone derivatives

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