78518-73-7

Usage

Uses

Used in Fragrance and Flavoring Industries:
(3R,9aα)-Decahydro-2,2,5aβ,7-tetramethyl-6β-[2-[(1R,3aR,5S,8aR)-1,2,3,3a,4,5,8,8a-octahydro-1-hydroxy-1,4,4,6-tetramethylazulen-5-yl]ethyl]-1-benzoxepine-3α,7β-diol is used as a key ingredient in the fragrance and flavoring industries for its distinctive aromatic qualities, adding unique scents and flavors to various products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3R,9aα)-Decahydro-2,2,5aβ,7-tetramethyl-6β-[2-[(1R,3aR,5S,8aR)-1,2,3,3a,4,5,8,8a-octahydro-1-hydroxy-1,4,4,6-tetramethylazulen-5-yl]ethyl]-1-benzoxepine-3α,7β-diol is being studied for its potential medicinal properties, with the aim of developing new treatments for various ailments based on its chemical characteristics and natural origin.
Used in Scientific Research:
This chemical compound is also of interest to researchers across various scientific fields due to its complex structure and potential applications, making it a subject of study for further understanding its properties and possible uses in different areas of science and technology.

InChI:InChI=1/C30H52O4/c1-19-9-10-22-21(13-17-29(22,7)32)26(2,3)20(19)11-12-23-28(6)16-14-24(31)27(4,5)34-25(28)15-18-30(23,8)33/h9,20-25,31-33H,10-18H2,1-8H3/t20-,21+,22+,23+,24+,25+,28+,29+,30-/m0/s1

Upstream product

• 78518-74-8 sipholenone A 

Downstream Products

• 132059-28-0 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (3S,5aS,6S,7R,9aS)-7-hydroxy-6-[2-((1S,3aS,5R,8aS)-1-hydroxy-1,4,4,6-tetramethyl-1,2,3,3a,4,5,8,8a-octahydro-azulen-5-yl)-ethyl]-2,2,5a,7-tetramethyl-decahydro-benzo[b]oxepin-3-yl ester 
• 133696-64-7 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (3S,5aS,6S,7R,9aS)-7-hydroxy-6-[2-((1S,3aS,5R,8aS)-1-hydroxy-1,4,4,6-tetramethyl-1,2,3,3a,4,5,8,8a-octahydro-azulen-5-yl)-ethyl]-2,2,5a,7-tetramethyl-decahydro-benzo[b]oxepin-3-yl ester 
• 1562411-56-6 sipholenol A-4-O-3′,4′-dichlorobenzoate 
• 1562411-57-7 C₃₇H₅₅NO₇ 
• 1562411-58-8 C₃₈H₅₅F₃O₅ 
• 1562411-59-9 C₃₇H₅₅ClO₅ 
• 1562411-60-2 4β-O-3′-nitrobenzoylsipholenol A 
• 1562411-61-3 C₃₇H₅₅FO₅ 
• 1562411-62-4 4β-O-3'-(trifluoromethyl)benzoylsipholenol A 
• 1562411-63-5 4β-O-3'-fluoro-5'-(trifluoromethyl)benzoylsipholenol A 
• 1562411-64-6 4β-O-4'-fluoro-5'-(trifluoromethyl)benzoylsipholenol A 
• 1562411-52-2 4β-O-5′-fluorobenzoylsipholenol A 
• 1562411-53-3 C₃₇H₅₅NO₇ 
• 1562411-54-4 C₃₈H₅₅F₃O₅ 

Relevant academic research and scientific papers

New triterpenoids from the red sea sponge Siphonochalina siphonella

Clear differences were found when comparing the chemical content of the northern, Gulf of Eilat, to the southern-central, Dahlak archipelago, Red Sea sponge Siphonochalina siphonella. The Dahlak sponge was found to be richer in the more polar triterpenes. Nine new compounds (1-4, 7, 8, 15-17) were isolated and identified, among them two sipholane glycosides, sipholenoside A and B (7 and 8), and one compound, dahabinone A (17), possessing a new skeleton.

The Sipholanes: A Novel Group of Triterpenes from the Marine Sponge Siphonochalina siphonella

Eight new squalene-derived triterpenes possessing a hitherto unknown framework have been isolated from the Red Sea sponge Siphonochalina siphonella.The novel skeleton, designated sipholane, consists of a cis-octahydroazulene linked via an ethylene bridge to a trans-decahydrobenzoxepine.The structure of the sipholane skeleton was established by an X-ray diffraction analysis of one of the natural compounds derivatives (16).The structure of the latter made possible the NMR and mass spectral interpretations and, hence, the structure elucidation of the additional seven new compounds.The structural determination were also assisted by various chemical correlations as well as transformations to compounds with well-defined functionalities.Of special interest is the suggested biogenesis of the sipholanes starting from 2,3:6,7:18,19-triepoxysqualene.In contrast to the single cyclization process that takes place in the biosynthesis of tetra- and pentacyclic triterpenes, the suggested route leading to the sipholanes involves two consecutive cyclizations.