CAS 1187925-31-0

Azuleno[6,5-b]furan-2(3H)-one,decahydro-4,5-dihydroxy-4a,8-dimethyl-3-methylene-, (3aS,4S,4aS,5S,7aS,8R,9aS)-

Description:

Azuleno[6,5-b]furan-2(3H)-one, decahydro-4,5-dihydroxy-4a,8-dimethyl-3-methylene-, with the CAS number 1187925-31-0, is a complex organic compound characterized by its unique fused ring structure that incorporates both azulene and furan moieties. This compound features multiple stereocenters, contributing to its chiral nature, which can influence its biological activity and interactions. The presence of hydroxyl groups indicates potential for hydrogen bonding, enhancing solubility in polar solvents and possibly affecting its reactivity. The decahydro framework suggests a saturated structure, which may impart stability and influence its physical properties, such as melting and boiling points. Additionally, the dimethyl and methylene substituents can affect the compound's sterics and electronic properties, potentially impacting its reactivity and interactions with other molecules. Overall, this compound's intricate structure and functional groups suggest it may have interesting applications in fields such as medicinal chemistry or materials science, although specific biological or chemical properties would require further investigation.

Formula: C₁₅H₂₂O₄

Synonyms:

• CarabrolactoneB

Carabrolactone B

CAS: 1187925-31-0

Formula: C₁₅H₂₂O₄

Purity: 98.5%

Molecular weight: 266.3328

Ref: IN-DA008YA5

Carabrolactone B

CAS: 1187925-31-0

Carabrolactone B is a natural product of Carpesium, Asteraceae.

Formula: C₁₅H₂₂O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 266.33

Ref: TM-TN3589

Carabrolactone B

CAS: 1187925-31-0

Formula: C₁₅H₂₂O₄

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 266.337

Ref: BP-SBP00076

Carabrolactone B

CAS: 1187925-31-0

Carabrolactone B is a synthetic compound, which is derived from the modification of natural lactone structures. It is primarily sourced through chemical synthesis, utilizing various organic chemistry techniques to produce the lactone framework. The mode of action of Carabrolactone B involves interaction with specific cellular targets, often influencing signaling pathways or enzyme activity. These interactions can lead to changes in cellular processes, such as apoptosis or proliferation, depending on the context.

Formula: C₁₅H₂₂O₄

Purity: Min. 95%

Molecular weight: 266.33 g/mol

Ref: 3D-MXB92531