
CAS 23811-08-7: Hinesol
Formula:C15H26O
InChI:InChI=1S/C15H26O/c1-11-6-5-7-12(2)15(11)9-8-13(10-15)14(3,4)16/h6,12-13,16H,5,7-10H2,1-4H3/t12-,13+,15+/m0/s1
InChI key:InChIKey=ICWHTQRTTHCUHW-GZBFAFLISA-N
SMILES:C[C@@H]1[C@]2(C[C@H]([C@@](C)(C)O)CC2)C(C)=CCC1
Synonyms:- (2R,5S,10S)-α,α,6,10-Tetramethylspiro[4.5]dec-6-ene-2-methanol
- Hinesol
- Spiro[4.5]dec-6-ene-2-methanol, α,α,6,10-tetramethyl-, (2R,5S,10S)-
- Spiro[4.5]dec-6-ene-2-methanol, α,α,6,10-tetramethyl-, [2R-[2α,5α(S*)]]-
- spiro[4.5]dec-6-ene-2-methanol, alpha,alpha,6,10-tetramethyl-, (2S,5R,10R)-
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Found 6 products.
Hinesol
CAS:Hinesol, a sesquiterpenoid from Atractylodes lancea, induces apoptosis in HL-60 cells via JNK pathway.Formula:C15H26OPurity:98%Color and Shape:SolidMolecular weight:222.37(2R,5S,10S)-α,α,6,10-Tetramethylspiro[4.5]dec-6-ene-2-methanol
CAS:(2R,5S,10S)-alpha,alpha,6,10-Tetramethylspiro[4.5]dec-6-ene-2-methanol is a sesquiterpene, which is a type of naturally occurring organic compound. It is typically sourced from plant essential oils and has been identified in various species as a component contributing to their chemically mediated interactions. The mode of action of this compound involves its role as a semiochemical, specifically acting as a pheromone. Sesquiterpenes like this one are integral in intra- and interspecies communication, often influencing behaviors such as aggregation, mating, and foraging. In terms of applications, this compound has been studied for its potential use in integrated pest management (IPM) strategies. By leveraging its pheromonal properties, scientists aim to develop more targeted and environmentally friendly approaches to controlling pest populations. This can lead to reduced reliance on traditional chemical pesticides, with benefits for agricultural sustainability and ecosystem health. Research continues into optimizing its use in various contexts, ensuring efficacy while minimizing unintended ecological impacts.Formula:C15H26OPurity:Min. 95%Molecular weight:222.37 g/mol