613239-75-1 Usage
Uses
Used in Organic Synthesis:
4-[5-(Trifluoromethyl)pyridin-2-yl]benzyl alcohol is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, enhancing the efficiency and selectivity of the processes involved.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-[5-(Trifluoromethyl)pyridin-2-yl]benzyl alcohol is utilized as an intermediate in the production of drugs. Its unique structure allows it to be a key component in the synthesis of medicinal compounds with specific therapeutic properties.
Used in Agrochemical Development:
4-[5-(Trifluoromethyl)pyridin-2-yl]benzyl alcohol also finds application in the agrochemical sector, where it serves as an intermediate in the synthesis of pesticides and other agricultural chemicals, contributing to the development of effective and targeted products for crop protection.
Used in Material Science:
In the field of material science, 4-[5-(Trifluoromethyl)pyridin-2-yl]benzyl alcohol is used as a building block for the development of new materials. Its structural features make it a valuable component in creating materials with novel properties and applications.
Used in Bioactive Molecule Synthesis:
4-[5-(Trifluoromethyl)pyridin-2-yl]benzyl alcohol is employed in the synthesis of bioactive molecules, where it contributes to the creation of compounds with potential biological activity, opening avenues for new drug discoveries and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 613239-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,3,2,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 613239-75:
(8*6)+(7*1)+(6*3)+(5*2)+(4*3)+(3*9)+(2*7)+(1*5)=141
141 % 10 = 1
So 613239-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H10F3NO/c14-13(15,16)11-5-6-12(17-7-11)10-3-1-9(8-18)2-4-10/h1-7,18H,8H2
613239-75-1Relevant academic research and scientific papers
Water-soluble palladacycles containing hydroxymethyl groups: Synthesis, crystal structures and use as catalysts for amination and Suzuki coupling of reactions
Han, Xin,Li, Hong-Mei,Xu, Chen,Xiao, Zhi-Qiang,Wang, Zhi-Qiang,Fu, Wei-Jun,Hao, Xin-Qi,Song, Mao-Ping
, p. 403 - 411 (2016/04/19)
Two water-soluble monophosphine [PPh3 and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl(Sphos)]-palladacycles containing hydroxymethyl groups 2-3 were prepared by cyclopalladation and chloride bridge-splitting reactions. The complexes were characterized by elemental analysis, ESI-MS and NMR. In addition, single-crystal X-ray analysis reveals that they have one-dimensional lamellar structures involving intermolecular hydrogen bonds and π-π interactions. The use of these palladacycles as catalysts for amination and Suzuki coupling of aryl chlorides in water was investigated. Complex 3 was found to be very efficient for these coupling reactions. Additionally, it was also successfully used in Suzuki coupling of (hydroxymethyl)phenylboronic acid for the synthesis of substituted 2-N-heterocyclic biarylmethanols.
Compounds that modulate PPAR activity and methods for their preparation
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Page 32, (2010/02/05)
This invention discloses compounds that alter PPAR activity. The invention also discloses pharmaceutically acceptable salts of the compounds, pharmaceutically acceptable compositions comprising the compounds or their salts, and methods of using them as therapeutic agents for treating or preventing disipidemia, hypercholesteremia, obesity, eating disorders, hyperglycemia, atherosclerosis, hypertriglyceridemia, hyperinsulinemia and diabetes in a mammal as well as methods of supressing appetite and modulating leptin levels in a mammal. The present invention also discloses methods for making the disclosed compounds.
