CAS 14348-16-4
:Poriol
Description:
Poriol, identified by the CAS number 14348-16-4, is a chemical compound that belongs to the class of organic substances. It is characterized by its unique molecular structure, which contributes to its specific chemical properties and potential applications. Poriol is typically recognized for its role in various chemical reactions and may exhibit properties such as solubility in certain solvents, reactivity with other chemical species, and stability under specific conditions. The compound may also possess functional groups that influence its behavior in biological systems or industrial processes. While detailed information on its applications and safety profile may vary, it is essential to handle Poriol with care, following appropriate safety guidelines, as with any chemical substance. For precise applications, safety data, and handling procedures, consulting material safety data sheets (MSDS) and relevant literature is recommended.
Formula:C16H14O5
InChI:InChI=1S/C16H14O5/c1-8-11(18)6-14-15(16(8)20)12(19)7-13(21-14)9-2-4-10(17)5-3-9/h2-6,13,17-18,20H,7H2,1H3/t13-/m0/s1
InChI key:InChIKey=SLFZBNOERHGNMI-ZDUSSCGKSA-N
SMILES:O=C1C=2C(O[C@@H](C1)C3=CC=C(O)C=C3)=CC(O)=C(C)C2O
Synonyms:- 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-, (S)-
- 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-, (2S)-
- (2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-4H-1-benzopyran-4-one
- Poriol
- 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methyl-2,3-dihydro-4H-chromen-4-one
- Flavanone, 4′,5,7-trihydroxy-6-methyl-
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Found 5 products.
Poriol
CAS:Poriol is a natural product from Cephalotaxus sinensis.Formula:C16H14O5Purity:99.15%Color and Shape:SolidMolecular weight:286.28Poriol
CAS:<p>Poriol is a sesquiterpene lactone, which is a naturally occurring organic compound extracted from specific plant species. This compound exhibits potent biological activity through its interaction with multiple cellular signaling pathways. Its mode of action primarily involves the inhibition of pathways such as NF-kB and STAT3, which play crucial roles in the regulation of inflammation and cancer progression.</p>Formula:C16H14O5Purity:Min. 95%Molecular weight:286.28 g/mol




