CAS 104273-73-6

4-(Cyclopropylcarbonyl)-3,5-dioxocyclohexanecarboxylic acid

Description:

4-(Cyclopropylcarbonyl)-3,5-dioxocyclohexanecarboxylic acid, with the CAS number 104273-73-6, is a chemical compound characterized by its unique bicyclic structure and functional groups. This substance features a cyclohexane ring with two carbonyl (C=O) groups at the 3 and 5 positions, contributing to its dioxo classification. The presence of a cyclopropylcarbonyl group at the 4 position introduces additional steric and electronic effects, influencing its reactivity and potential applications. The carboxylic acid functional group enhances its acidity and solubility in polar solvents, making it suitable for various chemical reactions, including esterification and amidation. This compound may exhibit interesting biological activities, which could be explored in pharmaceutical research. Its structural complexity and functional diversity suggest potential utility in organic synthesis and medicinal chemistry. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

Formula: C₁₁H₁₂O₅

InChI: InChI=1S/C11H12O5/c12-7-3-6(11(15)16)4-8(13)9(7)10(14)5-1-2-5/h5-6,9H,1-4H2,(H,15,16)

InChI key: InChIKey=UNMYTEORJFXQBK-UHFFFAOYSA-N

SMILES: C(=O)(C1C(=O)CC(C(O)=O)CC1=O)C2CC2

Synonyms:

• Cyclohexanecarboxylic acid, 4-(cyclopropylcarbonyl)-3,5-dioxo-
• 4-(Cyclopropylcarbonyl)-3,5-dioxocyclohexanecarboxylic acid

Trinexapac

CAS: 104273-73-6

Formula: C₁₁H₁₂O₅

Molecular weight: 224.21

Ref: 4Z-T-234004

Trinexapac

CAS: 104273-73-6

Trinexapac is an acylating agent that is processed by the enzyme lysine methyltransferase. It acts as a competitive inhibitor to the enzyme, preventing the transfer of methyl groups from S-adenosylmethionine to lysine residues in proteins. Trinexapac has been shown to inhibit fungal growth and prevent plant damage in cell culture studies. The mechanism of action of trinexapac may be due to its ability to inhibit protein synthesis by inhibiting acylation reactions and polymerase chain reactions. Trinexapac has also been shown to have a protective effect against photosynthetic pigments, which may be due to its ability to inhibit lipid peroxidation and oxidative stress.

Formula: C₁₁H₁₂O₅

Purity: Min. 95%

Molecular weight: 224.21 g/mol

Ref: 3D-EEA27373

4-(Cyclopropylcarbonyl)-3,5-dioxocyclohexanecarboxylic Acid

Controlled Product

CAS: 104273-73-6

Formula: C₁₁H₁₂O₅

Color and Shape: Neat

Molecular weight: 224.21

Ref: TR-C267210