CAS 3913-99-3

Methyl 4-methyl-3-oxocyclohexanecarboxylate

Description:

Methyl 4-methyl-3-oxocyclohexanecarboxylate, with the CAS number 3913-99-3, is an organic compound characterized by its cyclohexane ring structure, which features a ketone and an ester functional group. This compound typically appears as a colorless to pale yellow liquid and is known for its pleasant, fruity odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic cyclohexane framework. The presence of the methyl and carbonyl groups contributes to its reactivity, making it a potential intermediate in organic synthesis. Its chemical properties allow it to participate in various reactions, including nucleophilic additions and condensation reactions. Methyl 4-methyl-3-oxocyclohexanecarboxylate may be used in the synthesis of pharmaceuticals, agrochemicals, and flavoring agents, highlighting its versatility in chemical applications. As with many organic compounds, proper handling and safety precautions are essential due to potential health hazards associated with exposure.

Formula: C₉H₁₄O₃

InChI: InChI=1S/C9H14O3/c1-6-3-4-7(5-8(6)10)9(11)12-2/h6-7H,3-5H2,1-2H3

InChI key: InChIKey=HOXHPJRXOROTQC-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1CC(=O)C(C)CC1

Synonyms:

• Methyl 4-methyl-3-oxocyclohexanecarboxylate
• Cyclohexanecarboxylic acid, 4-methyl-3-oxo-, methyl ester
• NSC 99212

Methyl 4-methyl-3-oxocyclohexane-1-carboxylate

CAS: 3913-99-3

Methyl 4-methyl-3-oxocyclohexane-1-carboxylate (MMHCC) is an organic compound that is a member of the group of epoxides. It can be used as a reagent for transesterification reactions, such as the conversion of alcohols to ethers. MMHCC can also be used as a catalyst for hydrocarbon synthesis and as an isomerization agent. This chemical has been shown to catalytically convert alcohols to hydrocarbons and alkoxides, which are useful in the production of plastics.

Formula: C₉H₁₄O₃

Purity: Min. 95%

Molecular weight: 170.21 g/mol

Ref: 3D-DAA91399