CAS 15356-74-8

5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone

Description:

5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone, with CAS number 15356-74-8, is an organic compound characterized by its unique bicyclic structure that incorporates both furan and benzene moieties. This compound features a tetrahydrobenzofuran framework, which contributes to its stability and reactivity. It is typically a colorless to pale yellow liquid with a pleasant, sweet, and fruity aroma, making it of interest in the fragrance and flavor industry. The presence of multiple methyl groups enhances its hydrophobic properties and influences its volatility. In terms of solubility, it is generally more soluble in organic solvents than in water. The compound may exhibit various biological activities, although specific pharmacological properties would require further investigation. Its synthesis often involves cyclization reactions and can be derived from natural sources or synthesized in the laboratory. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards.

Formula: C₁₁H₁₆O₂

InChI: InChI=1S/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3

InChI key: InChIKey=IMKHDCBNRDRUEB-UHFFFAOYSA-N

SMILES: CC12C(=CC(=O)O1)C(C)(C)CCC2

Synonyms:

• (+/-)-(2,6,6,-Trimethyl-2-hydroxycyclohexylidene)acetic acid gamma-lactone
• (2,6,6-Trimethyl-2-Hydroxycyclohexylidene)Acetic Acid Lactone
• 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-
• 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (R)-
• 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (S)-
• 2,4,5,6,7,7a-Hexahydro-4,4,7a-trimethylbenzofuran-2-one
• 2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic acid lactone
• 4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one
• 4,5,7,7a-Tetrahydro-4,4,7a-trimethyl-2(6H)-benzofuranone
• 5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
• 5,8,7,7-Tetrahydro-4,4,7a-trimethyl-α-benzofuranone
• 9-Oxa-1,5,5-trimethylbicyclo[4.3.0]non-6-en-8-one
• Actinidiolide, dihydro-
• Dihydroactindiolide
• Dihydroactinolide

(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone

CAS: 15356-74-8

Formula: C₁₁H₁₆O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 180.2435

Ref: IN-DA00AQ6Y

4,4,7a-Trimethyl-5,6,7,7a-Tetrahydrobenzofuran-2(4H)-One

CAS: 15356-74-8

4,4,7a-Trimethyl-5,6,7,7a-Tetrahydrobenzofuran-2(4H)-One

Purity: 97%

Molecular weight: 180.24g/mol

Ref: 54-OR1011246

Dihydroactindiolide

CAS: 15356-74-8

Formula: C₁₁H₁₆O₂

Purity: 95%~99%

Molecular weight: 180.247

Ref: BP-BP4480

(±)-Dihydroactinidiolide

CAS: 15356-74-8

Purity: 98%

Molecular weight: 180.12

Ref: 10-F556909

4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one

Controlled Product

CAS: 15356-74-8

Formula: C₁₁H₁₆O₂

Color and Shape: Neat

Molecular weight: 180.2435

Ref: TR-T896490

(±)-Dihydroactinidiolide

CAS: 15356-74-8

Dihydroactinidiolide is a naturally occurring carotenoid that is found in the plant genus Dactylis. It has been shown to have neuroprotective effects and anticarcinogenic properties. However, it also has genotoxic effects. Dihydroactinidiolide increases the activity of two enzymes, polymerase chain reaction (PCR) and ethyl decanoate, which are involved in DNA replication and lipid synthesis. The first enzyme is important for DNA synthesis, while the second enzyme is important for cell membrane formation. In addition to these cellular processes, dihydroactinidiolide also inhibits cell death in neuronal cells by inhibiting apoptosis-inducing factor (AIF) and caspase 3 activities. Primary cells were used to measure the effects of dihydroactinidiolide on AIF activity.

Formula: C₁₁H₁₆O₂

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 180.24 g/mol

Ref: 3D-FD158201