CAS 63335-25-1
:1-Nonanone,1-(2,6-dihydroxyphenyl)-9-(3,4-dihydroxyphenyl)-
Description:
1-Nonanone, 1-(2,6-dihydroxyphenyl)-9-(3,4-dihydroxyphenyl)-, also known by its CAS number 63335-25-1, is an organic compound characterized by its ketone functional group and a long carbon chain. This compound features a nonanone backbone, which consists of a nine-carbon chain with a carbonyl group (C=O) at one end, contributing to its classification as a ketone. The presence of two hydroxyl (-OH) groups on the phenyl rings indicates that it has significant potential for hydrogen bonding, which can influence its solubility and reactivity. The dihydroxyphenyl substituents suggest that this compound may exhibit antioxidant properties, making it of interest in various biological and chemical applications. Additionally, the structural complexity of this molecule may lead to interesting interactions in biological systems, potentially affecting its pharmacological profile. Overall, 1-Nonanone, 1-(2,6-dihydroxyphenyl)-9-(3,4-dihydroxyphenyl)- is a compound of interest in both synthetic and medicinal chemistry due to its unique structural features.
Formula:C21H26O5
InChI:InChI=1S/C21H26O5/c22-16-13-12-15(14-20(16)26)8-5-3-1-2-4-6-9-17(23)21-18(24)10-7-11-19(21)25/h7,10-14,22,24-26H,1-6,8-9H2
InChI key:InChIKey=HCOZRFYGIFMIEX-UHFFFAOYSA-N
SMILES:C(CCCCCCCCC1=CC(O)=C(O)C=C1)(=O)C2=C(O)C=CC=C2O
Synonyms:- 1-(2,6-Dihydroxyphenyl)-9-(3,4-dihydroxyphenyl)-1-nonanone
- Malabaricone C
- MalabariconeC
- Nsc 287968
- 1-Nonanone, 1-(2,6-dihydroxyphenyl)-9-(3,4-dihydroxyphenyl)-
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Found 5 products.
Malabaricone C
CAS:Malabaricone C is a bioactive chemical.Formula:C21H26O5Purity:99.38% - 99.48%Color and Shape:SolidMolecular weight:358.43Malabaricone C
CAS:<p>Malabaricone C is a bioactive compound which is extracted from the roots of trees belonging to the genus Myristica. These trees are well-known for producing a diverse array of secondary metabolites with unique biological activities. Derived primarily through careful extraction processes from these natural sources, Malabaricone C has been characterized by its distinct ability to modulate inflammatory pathways and exhibit antimicrobial properties. The compound is known to interfere with specific biochemical targets, potentially inhibiting the expression of pro-inflammatory cytokines and disrupting microbial cell mechanisms.</p>Formula:C21H26O5Purity:Min. 95%Color and Shape:SolidMolecular weight:358.43 g/mol




