42541-96-8 Usage
Uses
Used in Pharmaceutical Research:
7-(3-(R)-Hydroxy-5-oxo-1-cyclopenten-1-yl)-5-(Z)-heptenoic acid methyl ester is utilized as a research compound for exploring its potential biological activities. Its unique structure and functional groups may confer properties that are valuable in the development of new drugs or therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 7-(3-(R)-Hydroxy-5-oxo-1-cyclopenten-1-yl)-5-(Z)-heptenoic acid methyl este serves as a lead molecule for the design and synthesis of novel pharmaceuticals. Its cyclopentenyl and heptenyl moieties, along with the hydroxy and ketone groups, could be key in modulating its interactions with biological targets, making it a promising candidate for further investigation and optimization.
Used in Drug Development:
7-(3-(R)-Hydroxy-5-oxo-1-cyclopenten-1-yl)-5-(Z)-heptenoic acid methyl ester is employed as a precursor in the synthesis of more complex molecules with potential medicinal applications. Its reactivity and structural features may allow for the creation of derivatives with enhanced pharmacological properties.
Used in Biochemical Studies:
7-(3-(R)-Hydroxy-5-oxo-1-cyclopenten-1-yl)-5-(Z)-heptenoic acid methyl este is also used in biochemical research to understand its interactions with enzymes, receptors, or other biomolecules. Such studies can provide insights into its mechanism of action and potential therapeutic effects, which are crucial for its application in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 42541-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,4 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42541-96:
(7*4)+(6*2)+(5*5)+(4*4)+(3*1)+(2*9)+(1*6)=108
108 % 10 = 8
So 42541-96-8 is a valid CAS Registry Number.
42541-96-8Relevant academic research and scientific papers
Total synthesis of E1 and E2 isoprostanes by diastereoselective protonation
Rodríguez, Ana R.,Spur, Bernd W.
, p. 9249 - 9253 (2007/10/03)
A short total synthesis of the E-type isoprostanes has been achieved using a two-component coupling process combined with a diastereoselective protonation under reagent control. Mild cleavage of the silyl protective groups with cat. BiBr3 or HF/Py followed by enzymatic hydrolysis of the methyl ester afforded the free E-type isoprostanes.
A Novel Vinyl Anion Equivalent. An Extremely Short Synthesis of 2-Substituted 2-Cycloalkenones and Prostaglandin Key Intermediates via Destannylselenenylation
Kusuda, Shinya,Watanabe, Yoshihiko,Ueno, Yoshio,Toru, Takeshi
, p. 3145 - 3152 (2007/10/02)
The preparation of a novel vinyl anion equivalent and a new destannylselenenylation procedure are described.The conjugate addition of (tributylstannyl)lithium to 2-(phenylseleno)-2-cycloalkenones, followed by the trapping of the resulting enolates with al
An extremely short synthesis of the prostaglandin key intermediate through a novel vinyl anion equivalent
Kusuda, Shinya,Watanabe, Yoshihiko,Ueno, Yoshio,Toru, Takeshi
, p. 1325 - 1326 (2007/10/02)
A one-pot synthesis of the PGE2 key intermediate from 2-(phenylseleno)-2-cyclopentenone is described.
7-{3-Hydroxy-2β-[4-hydroxy-4-(lower alkyl)-trans-1-octen-1-yl]-5-oxocyclopent-1α-yl}hept-5-cis-enoic acids and related compounds
-
, (2008/06/13)
7-{3-Hydroxy-2β-[4-hydroxy-4-(lower alkyl)-trans-1-octen-1-yl]-5-oxocyclopent-1α-yl}hept-5-cis-enoic acids, displaying valuable pharmacological properties, e.g., gastric anti-secretory, are produced by the reaction of 7-(3-oxygenated-5-oxocyclopent-1-en-1-yl)hept-5-cis-enoic acid or ester with the appropriate organometallic reagent.
