CAS 189351-15-3

2-Cyclohexen-1-one,4-hydroxy-4-[(1E,3S)-3-hydroxy-1-butenyl]-3,5,5-trimethyl-, (4S)-

Description:

2-Cyclohexen-1-one, 4-hydroxy-4-[(1E,3S)-3-hydroxy-1-butenyl]-3,5,5-trimethyl-, (4S)-, identified by CAS number 189351-15-3, is an organic compound characterized by its complex structure featuring a cyclohexene ring with various functional groups. This compound contains a ketone group, a hydroxyl group, and a substituted butenyl chain, contributing to its reactivity and potential biological activity. The presence of multiple chiral centers indicates that it can exist in different stereoisomeric forms, which may influence its chemical behavior and interactions. Typically, compounds of this nature may exhibit properties such as solubility in organic solvents, potential for hydrogen bonding due to hydroxyl groups, and reactivity in various organic reactions. Its structural features suggest possible applications in fields such as pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. However, specific physical properties like melting point, boiling point, and solubility would require empirical data for precise characterization.

Formula: C₁₃H₂₀O₃

Synonyms:

• Corchoionol C
• 2-Cyclohexen-1-one, 4-hydroxy-4-[(1E,3S)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethyl-, (4S)-
• Corchoiol C
• Corchoionoside C aglycon

2-Cyclohexen-1-one, 4-hydroxy-4-[(1E,3S)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethyl-, (4S)-

CAS: 189351-15-3

Formula: C₁₃H₂₀O₃

Purity: 96.0%

Molecular weight: 224.2961

Ref: IN-DA002ICJ

Corchoionol C

CAS: 189351-15-3

Corchoionol C is a natural product for research related to life sciences. The catalog number is TN3698 and the CAS number is 189351-15-3.

Formula: C₁₃H₂₀O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 224.3

Ref: TM-TN3698

Corchoionol C

CAS: 189351-15-3

Formula: C₁₃H₂₀O₃

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 224.3

Ref: BP-SBP01991

Corchoionol C

CAS: 189351-15-3

Corchoionol C is an organic compound, which is a phytochemical derived from the bark of cork oak trees. It exhibits potent antimicrobial properties through its mode of action, which involves disrupting microbial cell membranes and inhibiting essential enzymatic processes within pathogenic organisms. This disruption leads to cell lysis and eventual microbial death, making it a promising candidate in the field of antimicrobial research.

Formula: C₁₃H₂₀O₃

Purity: Min. 95%

Molecular weight: 224.3 g/mol

Ref: 3D-PHA35115