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1429740-63-5

2-(2-chloro-4-fluorophenyl)-3-methylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429740-63-5 Structure

  • Basic information

    1. Product Name: 2-(2-chloro-4-fluorophenyl)-3-methylpyridine
    2. Synonyms: 2-(2-chloro-4-fluorophenyl)-3-methylpyridine
    3. CAS NO:1429740-63-5
    4. Molecular Formula:
    5. Molecular Weight: 221.662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429740-63-5.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-(2-chloro-4-fluorophenyl)-3-methylpyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-chloro-4-fluorophenyl)-3-methylpyridine(1429740-63-5)
    11. EPA Substance Registry System: 2-(2-chloro-4-fluorophenyl)-3-methylpyridine(1429740-63-5)

  • 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: 1429740-63-5(Hazardous Substances Data)

1429740-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429740-63-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,7,4 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1429740-63:
(9*1)+(8*4)+(7*2)+(6*9)+(5*7)+(4*4)+(3*0)+(2*6)+(1*3)=175
175 % 10 = 5
So 1429740-63-5 is a valid CAS Registry Number.

1429740-63-5Downstream Products

1429740-63-5Relevant articles and documents

Copper-catalyzed aromatic C-H bond halogenation with lithium halides under aerobic conditions

Mo, Song,Zhu, Yamin,Shen, Zengming

, p. 2756 - 2760 (2013/05/08)

A concise and practical Cu-catalyzed protocol for the preparation of chloro- and bromoarenes via C-H bond activation has been developed. The advantages of this strategy are the employment of cheap Cu(NO3) 2·3H2O, LiX and O2, and its compatibility with both electron-donating and electron-withdrawing substituents on aryl rings.

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