168644-93-7 Usage
Uses
Used in Organic Synthesis:
2,4,5-Trifluorobenzyl amine is used as a building block in organic synthesis for the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure with fluorine atoms and an amine group provides specific reactivity and properties that are valuable in the synthesis of complex organic molecules.
Used in Heterocyclic Compound Synthesis:
2,4,5-TRIFLUOROBENZYL AMINE is also utilized as a reagent in the synthesis of heterocyclic compounds, particularly in the formation of pyrazole and pyrazoline derivatives. The presence of the amine group allows for reactions that lead to the creation of these heterocyclic structures, which are important in medicinal chemistry and materials science.
Used in Coordination Chemistry:
2,4,5-Trifluorobenzyl amine has been studied for its potential use as a ligand in coordination chemistry. Its ability to form coordination complexes with metal ions can lead to the development of new catalysts and materials with specific properties.
Used in Fluorescent Organic Materials:
Furthermore, 2,4,5-trifluorobenzyl amine is considered as a building block for the development of fluorescent organic materials. The presence of fluorine atoms can influence the electronic properties of the molecule, making it suitable for applications in the design of fluorescent probes and sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 168644-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,6,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 168644-93:
(8*1)+(7*6)+(6*8)+(5*6)+(4*4)+(3*4)+(2*9)+(1*3)=177
177 % 10 = 7
So 168644-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3N/c8-5-2-7(10)6(9)1-4(5)3-11/h1-2H,3,11H2
168644-93-7Relevant academic research and scientific papers
The pattern of fluorine substitution affects binding affinity in a small library of fluoroaromatic inhibitors for carbonic anhydrase
Doyon, Jeffrey B.,Jain, Ahamindra
, p. 183 - 185 (2008/02/11)
(equation presented) A library of fluoroaromatic inhibitors of carbonic anhydrase has been found to bind in a manner dependent on both hydrophobicity and the pattern of substitution of the fluoroaromatic ring. All of the compounds in the library bind to the protein with Kd 3 nM. We have inferred two distinct binding modes from our data, which suggest two types of interactions that should be considered when designing fluorinated drugs.
