23599-46-4

Usage

Uses

Used in Pharmaceutical Industry:
[5R,(-)]-5-Acetoxy-5,5aα,6,7,8,9,9a,9b-octahydro-9bα-hydroxy-6,6,9aβ-trimethylnaphtho[1,2-c]furan-3(1H)-one is used as a potential active pharmaceutical ingredient for [application reason], leveraging its unique structural features and functional groups to target specific biological pathways or receptors.
Used in Research and Development:
In the research industry, [5R,(-)]-5-Acetoxy-5,5aα,6,7,8,9,9a,9b-octahydro-9bα-hydroxy-6,6,9aβ-trimethylnaphtho[1,2-c]furan-3(1H)-one serves as a valuable compound for [application reason], such as exploring its interactions with various biomolecules, assessing its potential as a probe for biological studies, or investigating its reactivity in chemical synthesis.

InChI:InChI=1/C17H24O5/c1-10(18)22-12-8-11-14(19)21-9-17(11,20)16(4)7-5-6-15(2,3)13(12)16/h8,12-13,20H,5-7,9H2,1-4H3

Upstream product

• 73879-03-5 C₁₈H₂₆O₆ 
• 74411-45-3 C₂₁H₂₇Cl₃O₈ 
• 74411-43-1 C₁₉H₂₃Cl₃O₇ 
• 74411-44-2 C₁₉H₂₅Cl₃O₇ 
• 71557-91-0 9α,11-carbonyldioxydrim-7-en-12-ol 
• 108-24-7 acetic anhydride 
• 16772-63-7 (5R,5aS,9aS,9bR)-5,9b-Dihydroxy-6,6,9a-trimethyl-5,5a,6,7,8,9,9a,9b-octahydro-1H-naphtho[1,2-c]furan-3-one 
• 137760-98-6 Acetic acid (3S,5R,9aS,9bS)-9b-hydroxy-3-methoxy-6,6,9a-trimethyl-1,3,5,5a,6,7,8,9,9a,9b-decahydro-naphtho[1,2-c]furan-5-yl ester 
• 137760-98-6 Acetic acid (3R,5R,9aS,9bS)-9b-hydroxy-3-methoxy-6,6,9a-trimethyl-1,3,5,5a,6,7,8,9,9a,9b-decahydro-naphtho[1,2-c]furan-5-yl ester 
• 137760-96-4 (3S,9aS,9bS)-9b-Hydroxy-3-methoxy-6,6,9a-trimethyl-1,5a,6,7,8,9,9a,9b-octahydro-3H-naphtho[1,2-c]furan-5-one 
• 137760-96-4 (3R,9aS,9bS)-9b-Hydroxy-3-methoxy-6,6,9a-trimethyl-1,5a,6,7,8,9,9a,9b-octahydro-3H-naphtho[1,2-c]furan-5-one 
• 137760-97-5 (3S,5R,9aS,9bS)-3-Methoxy-6,6,9a-trimethyl-3,5,5a,6,7,8,9,9a-octahydro-naphtho[1,2-c]furan-5,9b-diol 
• 137760-97-5 (3R,5R,9aS,9bS)-3-Methoxy-6,6,9a-trimethyl-3,5,5a,6,7,8,9,9a-octahydro-naphtho[1,2-c]furan-5,9b-diol 
• 137761-00-3 cinnamodial 12-ethylene acetal 

Relevant academic research and scientific papers

Synthetic studies on biologically active natural compounds. Part III. Stereospecific transformation of uvidin A into (-)-cinnamosmolide

The first synthesis of natural (-)-cinnamosmolide (1a) from the sesquiterpene uvidin A (3) is described, The important synthetic intermediates 12a-b were also obtained from (-)-cinnamodial (2).

SYNTHESES OF (+/-)-CINNAMODIAL AND (+/-)-CINNAMOSMOLIDE

Syntheses of (+/-)-cinnamodial and (+/-)-cinnamosmolide were achieved starting from the intermediate used in the synthesis of (+/-)-warburganal.