CAS 24909-95-3

Spiro[furan-3(2H),2'-[2H]inden]-2-one,decahydro-1',7'-dihydroxy-3'a,4'-dimethyl-4-methylene-,(1'R,2'R,3'aR,4'S,7'S,7'aR)-

Description:

Spiro[furan-3(2H),2'-[2H]inden]-2-one, with the CAS number 24909-95-3, is a complex organic compound characterized by its unique spirocyclic structure, which features a fused ring system comprising a furan and an indene moiety. This compound exhibits a decahydro configuration, indicating a fully saturated framework with multiple stereocenters, contributing to its chiral nature. The presence of hydroxyl groups (dihydroxy) suggests potential for hydrogen bonding, which may influence its solubility and reactivity. Additionally, the dimethyl and methylene substituents indicate that the compound has multiple alkyl groups, which can affect its physical properties such as boiling point and melting point. The stereochemistry, denoted by the specific R and S configurations, plays a crucial role in determining the compound's biological activity and interaction with other molecules. Overall, this compound's structural complexity and functional groups suggest it may have interesting chemical behavior and potential applications in fields such as medicinal chemistry or materials science.

Formula: C₁₅H₂₂O₄

Synonyms:

• Spiro[furan-3(2H),2'-[2H]inden]-2-one,decahydro-1',7'-dihydroxy-3'a,4'-dimethyl-4-methylene-, [1'R-(1'a,2'a,3'aa,4'a,7'b,7'aa)]-
• Spiro[furan-3(2H),2'-indan]-2-one, 3'a,4,4',5,5',6',7',7'ab-octahydro-1'b,7'a-dihydroxy-3'ab,4'b-dimethyl-4-methylene- (8CI)
• (-)-Bakkenolide III
• Fukinolidol

Bakkenolide III

CAS: 24909-95-3

Bakkenolide III may have cytotoxicity.

Formula: C₁₅H₂₂O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 266.337

Ref: TM-TN3485

Bakkenolide III

CAS: 24909-95-3

Formula: C₁₅H₂₂O₄

Purity: 95%~99%

Molecular weight: 266.337

Ref: BP-SBP04268

Bakkenolide III

CAS: 24909-95-3

Bakkenolide III is a bioactive sesquiterpene lactone, which is isolated from the plant Petasites japonicus, commonly known as butterbur. This compound is known for its significant pharmacological activities. The mode of action of Bakkenolide III primarily involves the inhibition of pro-inflammatory pathways, which results in its anti-inflammatory effects. It interferes with the activity of key signaling molecules involved in the inflammatory response, thereby modulating cellular processes that contribute to inflammation.

Formula: C₁₅H₂₂O₄

Purity: Min. 95%

Molecular weight: 266.33 g/mol

Ref: 3D-ZAA90995