CAS 227471-20-7
:1,4,5-Naphthalenetriol,decahydro-4,8a-dimethyl-6-(1-methylethyl)-, (1R,4S,4aS,5S,6S,8aR)-
Description:
1,4,5-Naphthalenetriol, decahydro-4,8a-dimethyl-6-(1-methylethyl)-, with the CAS number 227471-20-7, is a complex organic compound characterized by its polycyclic structure, which includes a naphthalene core modified with multiple hydroxyl groups and alkyl substituents. This compound features a saturated bicyclic framework, indicating that it has undergone hydrogenation, resulting in a decahydro configuration. The presence of three hydroxyl (-OH) groups suggests it may exhibit significant polarity and potential for hydrogen bonding, influencing its solubility and reactivity. The specific stereochemistry, denoted by the (1R,4S,4aS,5S,6S,8aR) notation, indicates the spatial arrangement of atoms, which can affect the compound's biological activity and interaction with other molecules. Such compounds may be of interest in fields like medicinal chemistry or materials science due to their unique structural properties and potential applications. However, detailed studies would be necessary to fully understand its chemical behavior and potential uses.
Formula:C15H28O3
Synonyms:- (+)-1b,4b,6a-Trihydroxyeudesmane
- Mucrolidin
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Found 4 products.
Mucrolidin
CAS:Mucrolidin shows weak antibacterial activity.Formula:C15H28O3Purity:98%Color and Shape:SolidMolecular weight:256.386Mucrolidin
CAS:Mucrolidin is a natural product compound, specifically an antibiotic, derived from a rare microbial species found in soil samples. This novel compound is synthesized by the unique metabolic pathways of the microorganism from which it is isolated. The mode of action of Mucrolidin involves inhibiting bacterial cell wall synthesis, thereby compromising the structural integrity of pathogenic bacteria. This interference leads to the disruption of cellular processes, causing bacterial cell death.Formula:C15H28O3Purity:Min. 95%Molecular weight:256.38 g/mol



