2402-67-7 Usage
Uses
Used in Pharmaceutical Industry:
2-(3-Amino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is used as a building block for the synthesis of various drugs and pharmaceutical intermediates. Its unique structure allows for the development of new compounds with potential therapeutic effects.
Used in Organic Chemistry:
2-(3-Amino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is used as a reagent in the synthesis of various organic compounds. Its fluorinated alcohol structure and amino group enable it to participate in a wide range of chemical reactions, contributing to the creation of new organic molecules.
Used in Materials Science:
2-(3-Amino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol has been studied for its potential applications in the field of materials science. Its unique properties may contribute to the development of new materials with specific characteristics for various uses.
Used as a Solvent in Chemical Reactions:
Due to its fluorinated alcohol nature, 2-(3-Amino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol can be used as a solvent in chemical reactions. Its ability to dissolve a variety of compounds and facilitate reaction processes makes it a valuable component in the synthesis of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 2402-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2402-67:
(6*2)+(5*4)+(4*0)+(3*2)+(2*6)+(1*7)=57
57 % 10 = 7
So 2402-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F6NO/c10-8(11,12)7(17,9(13,14)15)5-2-1-3-6(16)4-5/h1-4,17H,16H2
2402-67-7Relevant academic research and scientific papers
Discovery and optimization of a novel series of liver X receptor-α agonists
Li, Leping,Liu, Jiwen,Zhu, Liusheng,Cutler, Serena,Hasegawa, Hirohiko,Shan, Bei,Medina, Julio C.
, p. 1638 - 1642 (2007/10/03)
A novel series of hexafluorocarbinols were discovered as potent activators of the liver X receptor-α using a fluorescence polarization assay. Structure-activity relationship study led to the identification of compounds that are more potent agonists than t
