1197348-98-3 Usage
Description
3-methylbutyl (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate is a complex organic compound with a unique molecular structure. It is characterized by its chiral centers at the 3R and 5S positions, and a trans double bond at the 6E position. 3-methylbutyl (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate is derived from a class of molecules with potential pharmaceutical applications, particularly in the development of novel therapeutic agents.
Uses
Used in Pharmaceutical Industry:
3-methylbutyl (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate is used as a key intermediate in the synthesis of new drugs for the treatment of various diseases. Its unique structure and functional groups make it a promising candidate for the development of selective inhibitors or modulators of specific biological targets.
Used in Research and Development:
In the field of medicinal chemistry, this compound serves as a valuable research tool for understanding the structure-activity relationships of potential drug candidates. It can be used to explore the effects of different functional groups and stereochemistry on the biological activity of the molecule, ultimately leading to the optimization of drug candidates with improved efficacy and safety profiles.
Used in Drug Synthesis:
3-methylbutyl (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate can be employed as a building block in the synthesis of more complex drug molecules. Its versatile structure allows for further functionalization and modification, enabling the creation of a diverse range of compounds with tailored properties and applications.
It is important to note that the specific applications and uses of this compound may vary depending on the context and the ongoing research in the field. As our understanding of its properties and potential therapeutic effects evolves, new applications may be discovered, further expanding the utility of this unique molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 1197348-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,3,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1197348-98:
(9*1)+(8*1)+(7*9)+(6*7)+(5*3)+(4*4)+(3*8)+(2*9)+(1*8)=203
203 % 10 = 3
So 1197348-98-3 is a valid CAS Registry Number.
1197348-98-3Relevant articles and documents
3,5-dihydroxyhept-6-enoic acid derivative preparation method
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, (2017/04/19)
The invention relates to a preparation method of 3, 5-dihydroxy-6-heptenoic acid derivatives. The preparation method comprises the steps of hydrolyzing crude statin ester to form a water-soluble alkali metal salt, extracting by using a solvent to remove impurities which cannot be dissolved into water, and converting at high yield to form ester with relatively high purity; then, purifying the ester by using a recrystallization way to obtain pure statin ester; and finally, converting the pure statin ester at high yield to form statin calcium, namely the 3, 5-dihydroxy-6-heptenoic acid derivatives. The 3, 5-dihydroxy-6-heptenoic acid derivatives, namely rosuvastatin calcium and pitavastatin calcium, synthesized by using the preparation method are high in purity and total yield, relatively low in cost and beneficial to mass production.
