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2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 627510-99-0 Structure
  • Basic information

    1. Product Name: 2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol
    2. Synonyms: 2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol
    3. CAS NO:627510-99-0
    4. Molecular Formula:
    5. Molecular Weight: 278.233
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 627510-99-0.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: 2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol(627510-99-0)
    11. EPA Substance Registry System: 2-(4-trifluoromethylphenyl)-1H-pyrrolo[2,3-c]pyridin-1-ol(627510-99-0)
  • 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: 627510-99-0(Hazardous Substances Data)

627510-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 627510-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,5,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 627510-99:
(8*6)+(7*2)+(6*7)+(5*5)+(4*1)+(3*0)+(2*9)+(1*9)=160
160 % 10 = 0
So 627510-99-0 is a valid CAS Registry Number.

627510-99-0Relevant articles and documents

Synthesis of 2-aryl-1-hydroxyazaindoles and 2-arylazaindoles via oxidation of o-hydroxyaminostyrylpyridines

Kuzmich, Daniel,Mulrooney, Carol

, p. 1671 - 1678 (2007/10/03)

2-Aryl-1-hydroxyazaindoles (pyrrolopyridin-1-ols) are prepared via an oxidation/cyclization of o-hydroxyaminostyrylpyridines with DDQ. Reduction of the N-OH bond affords the corresponding 2-arylazaindoles (1H-pyrrolopyridines). The scope of the cyclization is explored via (i) the condensation of 4-methyl-3-nitropyridine with various aryl aldehydes to afford 2-aryl substituted 6-azaindoles and, (ii) the synthesis of 2-phenyl-4-, 5- and 7-azaindoles.

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