59632-76-7 Usage
Uses
Used in Pharmaceutical Industry:
(3aR,6E,10Z,14E,15aS)-2,3,3a,4,5,8,9,12,13,15a-Decahydro-6,14-dimethyl-3-methylene-2-oxocyclotetra-decab[b]furan-10-carboxylic acid is used as a potential bioactive compound for its unique structure and reactivity, which may contribute to the development of new pharmaceutical agents.
Used in Chemical Research:
This complex molecule is used in chemical research to study its reactivity, structural properties, and potential interactions with other molecules, providing insights into its possible applications and effects.
Used in Drug Development:
Due to its unique structure and reactivity, (3aR,6E,10Z,14E,15aS)-2,3,3a,4,5,8,9,12,13,15a-Decahydro-6,14-dimethyl-3-methylene-2-oxocyclotetradeca[b]furan-10-carboxylic acid may be used in drug development for the creation of novel therapeutic agents with specific biological activities.
Note: The specific applications and industries mentioned above are hypothetical and provided as examples based on the general properties of the compound. Further research and development would be necessary to determine the actual uses and effectiveness of (3aR,6E,10Z,14E,15aS)-2,3,3a,4,5,8,9,12,13,15a-Decahydro-6,14-dimethyl-3-methylene-2-oxocyclotetradeca[b]furan-10-carboxylic acid in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 59632-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59632-76:
(7*5)+(6*9)+(5*6)+(4*3)+(3*2)+(2*7)+(1*6)=157
157 % 10 = 7
So 59632-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O4/c1-13-6-4-8-16(19(21)22)9-5-7-14(2)12-18-17(11-10-13)15(3)20(23)24-18/h6,9,12,17-18H,3-5,7-8,10-11H2,1-2H3,(H,21,22)/b13-6+,14-12-,16-9-
59632-76-7Relevant academic research and scientific papers
CEMBRANOLIDE TOTAL SYNTHESIS. ANISOMELIC ACID
Marshall, James A.,DeHoff, Bradley S.
, p. 4849 - 4860 (2007/10/02)
The stereoselective total synthesis of (+/-)-anisomelic acid (34) has been achieved starting from aldehyde 7, the ozonolysis product of geranyl acetate.Two key steps ensured the stereoselectivity of the synthesis.The first entailed a highly anti-selective addition of the allyltitanium derived from carbamate 15 to aldehyde 5 affording the enol carbamate allylic alcohol 16.The second was a highly (Z)-selective Horner-Emmons cyclization of the derived phosphono ester aldehyde 25 leading to the conjugated ester 27.Further conversion led to the crystalline lactone 30 whose structure was confirmed through single crystal X-ray analysis.Equilibration of the conjugated double bond of 30 gave rise to a 1:1 mixture of the (Z) and (E) isomers.This result was foretold by molecular mechanics calculations.
STEREOSELECTIVE TOTAL SYNTHESIS OF THE CEMBRANOLIDE DITERPENE ANISOMELIC ACID
Marshall, James A.,DeHoff, Bradley S.
, p. 4873 - 4876 (2007/10/02)
A highly stereoselective total synthesis of the cembranolide diterpene anosomelic acid has been achieved via a convergent route.Macrocyclization was effected by a (Z)-selective intramolecular Horner-Emmons condensation.
