Welcome to LookChem.com Sign In|Join Free
  • or
2,3,6-trifluoro-N-phenylpyridin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1081978-32-6

Post Buying Request

1081978-32-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1081978-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1081978-32-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,1,9,7 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1081978-32:
(9*1)+(8*0)+(7*8)+(6*1)+(5*9)+(4*7)+(3*8)+(2*3)+(1*2)=176
176 % 10 = 6
So 1081978-32-6 is a valid CAS Registry Number.

1081978-32-6Downstream Products

1081978-32-6Relevant academic research and scientific papers

Hydrogen Bond Directed Photocatalytic Hydrodefluorination and Methods of Use Thereof

-

Sheet 4, (2021/01/22)

Methods of synthesizing compounds comprising fluorinated aryl groups are disclosed, wherein said methods utilize hydrogen bond directed photocatalytic hydrodefluorination.

Hydrogen Bond Directed Photocatalytic Hydrodefluorination: Overcoming Electronic Control

Khaled, Mohammad B.,El Mokadem, Roukaya K.,Weaver, Jimmie D.

, p. 13092 - 13101 (2017/09/26)

The photocatalytic C-F functionalization of highly fluorinated arenes is a powerful method for accessing functionalized multifluorinated arenes. The decisive step in the determining regioselectivity in fluorine functionalization is fluoride fragmentation from the radical anion of the multifluorinated arene. To date, the availability of regioisomers has been dictated by the innate electronics of the fluorinated arene, limiting the synthetic utility of the chemistry. This study investigates the remarkable ability of a strategically located hydrogen bond to transcend the normal regioselectivity of the C-F functionalization event. A significant rate acceleration is additionally observed for hydrodefluorination of fluorines that can undergo intramolecular hydrogen bonds that form 5-8-membered cycles with moderately acidic N-H's. The hydrogen bond is expected to facilitate the fragmentation not only by bending the C-F bond of the radical anion out of planarity but also by increasing the exothermicity of the fluoride extrusion step through protonation of the naked fluoride. Finally, the synthetic utility of the method is demonstrated in an expedited synthesis of the trifluorinated α-phenyl acetic acid derivative required for the commercial synthesis of Januvia, an antidiabetic drug. This represents the first synthesis of a commercially important multifluorinated arene via a defluorination strategy and is significantly shorter than the current strategy.

Mechanisms of reactions of halogenated compounds. Part 7. Effects of fluorine and other groups as substituents on nucleophilic aromatic substitution

Chambers, Richard D.,Martin, Peter A.,Sandford, Graham,Williams, D. Lyn H.

experimental part, p. 998 - 1002 (2009/04/04)

The effect of fluorine as a substituent group on nucleophilic aromatic substitution is discussed, where a fluorine atom located ortho to the point of substitution may be of variable activating influence, whereas fluorine located para is slightly deactivat

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1081978-32-6