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5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 861206-23-7 Structure
  • Basic information

    1. Product Name: 5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE
    2. Synonyms: 5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE;5,7-dibromo-1H,2H,3H-cyclopenta[b]quinoline
    3. CAS NO:861206-23-7
    4. Molecular Formula: C12H9Br2N
    5. Molecular Weight: 327.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 861206-23-7.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: 5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE(861206-23-7)
    11. EPA Substance Registry System: 5,7-DIBROMO-2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLINE(861206-23-7)
  • 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: 861206-23-7(Hazardous Substances Data)

861206-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861206-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,2,0 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 861206-23:
(8*8)+(7*6)+(6*1)+(5*2)+(4*0)+(3*6)+(2*2)+(1*3)=147
147 % 10 = 7
So 861206-23-7 is a valid CAS Registry Number.

861206-23-7Downstream Products

861206-23-7Relevant articles and documents

A novel enzymatic synthesis of quinoline derivatives

Zheng, Hui,Liu, Juan,Mei, Yi Jia,Shi, Qiao Yue,Zhang, Peng Fei

, p. 573 - 577 (2012)

A new mild enzymatic methodology for synthesizing quinoline derivatives by Friedlaender condensation was developed. A series of quinoline derivatives were synthesized and characterized by 1H NMR, 13C-NMR, IR and MS. The probable enzymatic mechanism was proposed. It provides a novel method to prepare quinoline derivatives.

Rapid and efficient synthesis of poly-substituted quinolines assisted by p-toluene sulphonic acid under solvent-free conditions: Comparative study of microwave irradiation versus conventional heating

Jia, Cheng-Sheng,Zhang, Ze,Tu, Shu-Jiang,Wang, Guan-Wu

, p. 104 - 110 (2007/10/03)

A rapid and efficient method for the preparation of various poly-substituted quinolines has been developed through the Friedlaender condensation of 2-aminoarylketone or 2-aminoarylaldehyde with carbonyl compounds in the presence of p-toluene sulphonic aci

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