75716-76-6 Usage
Uses
Used in Medicinal Chemistry:
(R)-methyl 3-((1R,3aS,7aR,E)-4-((Z)-2-((S)-5-hydroxy-2-methylenecyclohexylidene)ethylidene)-7a-methyloctahydro-1H-inden-1-yl)butanoate is used as a compound in medicinal chemistry for its potential to be a building block for pharmaceuticals due to its complex structure and various functional groups.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-methyl 3-((1R,3aS,7aR,E)-4-((Z)-2-((S)-5-hydroxy-2-methylenecyclohexylidene)ethylidene)-7a-methyloctahydro-1H-inden-1-yl)butanoate is used as a starting material or intermediate for synthesizing more complex organic compounds, taking advantage of its reactive functional groups.
Used in Chemical Research:
(R)-methyl 3-((1R,3aS,7aR,E)-4-((Z)-2-((S)-5-hydroxy-2-methylenecyclohexylidene)ethylidene)-7a-methyloctahydro-1H-inden-1-yl)butanoate is used as a subject of study in chemical research to understand its properties, reactivity, and potential applications in various chemical processes.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, (R)-methyl 3-((1R,3aS,7aR,E)-4-((Z)-2-((S)-5-hydroxy-2-methylenecyclohexylidene)ethylidene)-7a-methyloctahydro-1H-inden-1-yl)butanoate is used as a compound with potential therapeutic applications, possibly due to its complex structure and the presence of various functional groups that may interact with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 75716-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,1 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75716-76:
(7*7)+(6*5)+(5*7)+(4*1)+(3*6)+(2*7)+(1*6)=156
156 % 10 = 6
So 75716-76-6 is a valid CAS Registry Number.
75716-76-6Relevant academic research and scientific papers
Synthesis and biological evaluation of calcioic acid
Arnold, Leggy A.,Di Milo, Elliot S.,Mutchie, Tania R.,Yu, Olivia B.
, (2019/11/25)
Herein, we describe the synthesis of calcioic acid following a recently developed synthetic strategy for calcitroic acid. Several improvements to reaction conditions were made, which resulted in higher yields. The improved workup and isolation procedures
