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3-Benzothiazol-2-yl-quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 165067-13-0 Structure
  • Basic information

    1. Product Name: 3-Benzothiazol-2-yl-quinoline
    2. Synonyms: 3-Benzothiazol-2-yl-quinoline
    3. CAS NO:165067-13-0
    4. Molecular Formula: C17H11N3O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 165067-13-0.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: 3-Benzothiazol-2-yl-quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Benzothiazol-2-yl-quinoline(165067-13-0)
    11. EPA Substance Registry System: 3-Benzothiazol-2-yl-quinoline(165067-13-0)
  • 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: 165067-13-0(Hazardous Substances Data)

165067-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165067-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,0,6 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 165067-13:
(8*1)+(7*6)+(6*5)+(5*0)+(4*6)+(3*7)+(2*1)+(1*3)=130
130 % 10 = 0
So 165067-13-0 is a valid CAS Registry Number.

165067-13-0Downstream Products

165067-13-0Relevant articles and documents

Reactions of quinazolinium salts with quaternary heterocyclic salts yielding 3-hetarylquinolines

Gromov,Razinkin,Drach,Sergeev

, p. 1179 - 1185 (1998)

A novel type of transformations of the pyrimidine ring under the action of C-nucleophiles was found and a new method was developed for the synthesis of 3-hetarylquinolines from quinazoline derivatives and quaternary heterocyclic salts. An independent synthesis was carried out and transformations of one of the probable intermediates were studied. By-products were isolated. The effects of the nature of the heterocycle and substituents on the course of the ring transformation reaction were found, and the mechanism of the reaction was suggested.

High-Throughput Screening Protocol for the Coupling Reactions of Aryl Halides Using a Colorimetric Chemosensor for Halide Ions

Eom, Min Sik,Noh, Jieun,Kim, Han-Sung,Yoo, Soyeon,Han, Min Su,Lee, Sunwoo

supporting information, p. 1720 - 1723 (2016/05/19)

Mercury complex of 4-(2-pyridylazo)resorcinol (PAR-2Hg2+), a halide-ion chemosensor, was prepared and its efficiency as a tool for high-throughput screening (HTS) of transition-metal-catalyzed coupling reactions was investigated. It showed a high selectivity for halide ions. When the PAR-2Hg2+ complex was used in the Suzuki coupling reaction and C-H activated coupling reaction with aryl bromides, the quantitative and qualitative conversions of aryl halides were obtained from the reaction mixture color change.

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