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  • 1391025-82-3 Structure
  • Basic information

    1. Product Name: 3,6-F2-PN
    2. Synonyms: 3,6-F2-PN
    3. CAS NO:1391025-82-3
    4. Molecular Formula:
    5. Molecular Weight: 208.982
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1391025-82-3.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: 3,6-F2-PN(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,6-F2-PN(1391025-82-3)
    11. EPA Substance Registry System: 3,6-F2-PN(1391025-82-3)
  • 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: 1391025-82-3(Hazardous Substances Data)

1391025-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391025-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,0,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1391025-82:
(9*1)+(8*3)+(7*9)+(6*1)+(5*0)+(4*2)+(3*5)+(2*8)+(1*2)=143
143 % 10 = 3
So 1391025-82-3 is a valid CAS Registry Number.

1391025-82-3Downstream Products

1391025-82-3Relevant articles and documents

Synthesis of 6-Aryl-5-fluoropicolinate Herbicides via Halex Reaction of Tetrachloropicolinonitrile

Whiteker, Gregory T.,Froese, Robert D. J.,Arndt, Kim E.,Renga, James M.,Zhu, Yuanming,Roth, Gary A.,Yang, Qiang,Canturk, Belgin,Klosin, Jerzy

, p. 2166 - 2174 (2019)

The development of a new synthesis of 6-aryl-5-fluoropicolinate herbicides is described. This general route employs the halogen exchange (halex) reaction of tetrachloropicolinonitrile to give a mixture of chlorofluoropicolinonitriles. It was found that th

PROCESS FOR THE PREPARATION OF 4-AMINO-3-CHLORO-5-FLUORO-6-(SUBSTITUTED) PICOLINATES

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Page/Page column 7, (2012/07/31)

4-Amino-3-chloro-5-fluoro-6-(substituted)picolinates are conveniently prepared from 3,4,5,6-tetrachloropicolinonitrile by a series of steps involving fluorine exchange, amination, halogen exchange and hydrolysis, esterification and transition metal assist

PROCESS FOR THE PREPARATION OF 4-AMINO-3-CHLORO-5-FLUORO-6-(SUBSTITUTED) PICOLINATES

-

Page/Page column 7, (2012/07/31)

4-Amino-3-chloro-5-fluoro-6-(substituted)picolinates are conveniently prepared from 3,4,5,6-tetrachloropicolinonitrile by a series of steps involving fluorine exchange, amination, reaction with hydrazine, halogenation, hydrolysis and esterification, and t

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