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CAS 17092-92-1

:

(-)-Dihydroactinidiolide

Description:
(-)-Dihydroactinidiolide is a naturally occurring organic compound classified as a lactone, specifically a cyclic ester. It is derived from the fruit of the kiwifruit (Actinidia deliciosa) and is known for its pleasant, fruity aroma, which contributes to its use in flavoring and fragrance applications. The compound has a chiral center, resulting in its designation as the (-)-enantiomer, which is significant in the context of its sensory properties and potential biological activity. Its molecular structure features a six-membered ring, which is characteristic of many lactones, and it exhibits solubility in organic solvents. (-)-Dihydroactinidiolide has garnered interest in the fields of food science and perfumery due to its appealing scent profile. Additionally, research into its potential health benefits and applications in natural product synthesis continues to expand, highlighting its relevance in both industrial and academic settings. As with many organic compounds, safety and handling precautions should be observed when working with this substance.
Formula:C11H16O2
InChI:InChI=1S/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3/t11-/m1/s1
InChI key:InChIKey=IMKHDCBNRDRUEB-LLVKDONJSA-N
SMILES:C[C@@]12C(=CC(=O)O1)C(C)(C)CCC2
Synonyms:
  • (+/-)-(2,6,6,-Trimethyl-2-hydroxycyclohexylidene)acetic acid gamma-lactone
  • (2,6,6-Trimethyl-2-Hydroxycyclohexylidene)Acetic Acid Lactone
  • (7AR)-4,4,7a-trimethyl-2,4,5,6,7,7a-hexahydro-1-benzofuran-2-one
  • (7aR)-5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
  • (R)-5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
  • (R)-Dihydroactinidiolide
  • 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-
  • 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aR)-
  • 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (R)-
  • 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (S)-
  • See more synonyms
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Found 7 products.
  • 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aR)-

    CAS:
    Formula:C11H16O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:180.2435

    Ref: IN-DA00HZID

    5g
    150.00€
    25g
    559.00€
    250mg
    64.00€
  • Dihydroactinidiolide

    CAS:
    <p>Dihydroactinidiolide</p>
    Purity:≥98%
    Molecular weight:180.24g/mol

    Ref: 54-BUP15982

    1g
    258.00€
    25mg
    57.00€
    50mg
    80.00€
    100mg
    100.00€
    500mg
    213.00€
  • (2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone

    CAS:
    <p>(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone</p>
    Purity:98% 99%ee
    Molecular weight:180.24g/mol

    Ref: 54-OR927125

    1g
    350.00€
    5g
    1,179.00€
    100mg
    87.00€
    250mg
    150.00€
  • Dihydroactinidiolide

    CAS:
    <p>Dihydroactinidiolide (R-(-)Dihydro actinidiolide)is avolatileterpene. It has a sweet,tea-likeodorand is used as a fragrance.</p>
    Formula:C11H16O2
    Purity:99.94%
    Color and Shape:Less Crystal Colorless Crystal
    Molecular weight:180.24
  • R-Dihydroactinidiolide

    Controlled Product
    CAS:
    Formula:C11H16O2
    Color and Shape:Neat
    Molecular weight:180.244

    Ref: TR-R268145

    1g
    115.00€
    250mg
    87.00€
    500mg
    98.00€
  • 4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one

    CAS:
    Formula:C11H16O2
    Purity:95.0%
    Color and Shape:Solid
    Molecular weight:180.247

    Ref: 10-F209846

    1g
    16.00€
    5g
    38.00€
    10g
    65.00€
    25g
    119.00€
  • R-Dihydroactinidiolide

    CAS:
    <p>R-Dihydroactinidiolide is a carotenoid found in tobacco. It has been shown to inhibit the growth of neuroblastoma cells and other carcinoma cell lines in vitro, as well as to induce DNA damage and apoptosis in these cells. The surface methodology used for this study provides evidence that dihydroactinidiolide binds to specific receptors on the surface of cancer cells, which may be involved in the genotoxic effects observed. R-Dihydroactinidiolide can be metabolized by various enzymes into different metabolites with different biochemical properties and biological activities. This process involves cleavage of the acetate side chain by an enzyme called lipoxygenase, followed by oxidation of one or more double bonds on the ring system. The reaction mechanism is not yet known.</p>
    Formula:C11H16O2
    Purity:Min. 95%
    Color and Shape:Powder
    Molecular weight:180.24 g/mol

    Ref: 3D-FD33930

    2g
    288.00€
    5g
    375.00€
    10g
    468.00€
    25g
    735.00€