3512-18-3 Usage
Description
2,3,6-Trifluoropyridine is a colorless liquid that serves as a versatile intermediate in various organic syntheses and pharmaceutical applications due to its unique chemical properties.
Uses
Used in Organic Syntheses:
2,3,6-Trifluoropyridine is used as a key intermediate for the synthesis of various organic compounds. Its presence in the molecular structure can impart specific reactivity and properties to the final products, making it a valuable component in the development of new organic materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,6-trifluoropyridine is utilized as a building block for the development of novel drugs. Its unique fluorinated structure can enhance the pharmacokinetic and pharmacodynamic properties of the resulting drug candidates, potentially leading to improved therapeutic outcomes.
Chemical Properties:
As a colorless liquid, 2,3,6-trifluoropyridine exhibits distinct chemical properties that make it suitable for a wide range of applications in both organic synthesis and pharmaceutical development. Its fluorinated nature allows for specific reactivity and interaction with other molecules, contributing to its utility in creating new compounds and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 3512-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3512-18:
(6*3)+(5*5)+(4*1)+(3*2)+(2*1)+(1*8)=63
63 % 10 = 3
So 3512-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H2F3N/c6-3-1-2-4(7)9-5(3)8/h1-2H
3512-18-3Relevant articles and documents
Rhodium catalyzed, carbon-hydrogen bond directed hydrodefluorination of fluoroarenes
Ekkert, Olga,Strudley, Sebastian D. A.,Rozenfeld, Alisa,White, Andrew J. P.,Crimmin, Mark R.
supporting information, p. 7027 - 7030 (2015/05/19)
[CpRhCl(μ-Cl)]2 is reported as a highly efficient and selective precatalyst for the hydrodefluorination of perfluoroarenes using a hydrocarbon-soluble aluminum dihydride as the terminal reductant. Reactions are directed to cleave a C-F bond adjacent to an existing C-H bond with high regioselectivity (98.5-99%). A heterobimetallic complex containing an extremely rare Al-H-Rh functional group has been isolated and shown to be catalytically competent.
Heterocyclic derivatives
-
, (2008/06/13)
The invention relates to heterocyclic derivatives of the formula I wherein R1, A1, Z1, n, A2, Z2, Q1, Q2, Q3 and L have the meaning given in claim 1 and to their use as components of liquid crystalline media for electro-optical displays.
