1597407-58-3 Usage
Description
3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone is a complex organic compound characterized by its unique arrangement of a piperidine ring, an azetidine ring, and a trifluorophenyl group. The molecule features a hydroxy group and a ketone functional group, and it is a chiral compound due to the presence of stereocenters. This intricate chemical structure suggests potential pharmacological properties and possible applications in the pharmaceutical industry.
Uses
Used in Pharmaceutical Applications:
3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone is used as a potential therapeutic agent for various medical conditions due to its complex structure and chiral nature. 3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone's specific application would depend on further research and analysis to determine its pharmacological properties and efficacy.
Used in Drug Development Research:
In the field of drug development, 3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone can be used as a starting point for the synthesis of new drugs. Its unique structure may serve as a template for designing molecules with specific biological activities, targeting various diseases and conditions.
Used in Chemical Synthesis:
3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone can also be utilized in chemical synthesis as a building block or intermediate for creating other complex organic molecules. Its functional groups and chiral centers may allow for further chemical reactions to produce a variety of derivatives with different properties and applications.
Used in Analytical Chemistry:
3-hydroxy-3-[(S)-1-((S)-2-hydroxy-1-phenyl-ethyl)-piperidin-2-yl]-azetidin-1-yl-(2,3,4-trifluoro-phenyl)-methanone's chiral nature and complex structure make it a potential candidate for use in analytical chemistry, particularly in the development of chiral stationary phases for high-performance liquid chromatography (HPLC) or other separation techniques. This could be useful for the enantiomeric separation and analysis of chiral compounds in various industries, including pharmaceuticals, agrochemicals, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 1597407-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,7,4,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1597407-58:
(9*1)+(8*5)+(7*9)+(6*7)+(5*4)+(4*0)+(3*7)+(2*5)+(1*8)=213
213 % 10 = 3
So 1597407-58-3 is a valid CAS Registry Number.
1597407-58-3Relevant articles and documents
CRYSTALLINE FUMARATE SALT OF (S)-[3,4-DIFLUORO-2-(2-FLUORO-4-IODOPHENYLAMINO)PHENYL] [3-HYDROXY-3-(PIPERIDIN-2-YL) AZETIDIN-1-YL]-METHANONE
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, (2017/01/26)
This disclosure relates to the crystalline fumarate salt of (S)-[3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl] [3-hydroxy-3-(piperidin-2-yl) azetidin-l-yl]-methanone. The disclosure also relates to pharmaceutical compositions comprising the crystalline fumarate salt of (S)-[3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl] [3-hydroxy-3-(piperidin-2-yl) azetidin-l-yl]-methanone. The disclosure also relates to methods of treating cancers comprising administering to a patient in need thereof the crystalline fumarate salt of (S)-[3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl] [3-hydroxy-3-(piperidin-2-yl) azetidin-1-yl]-methanone.
