CAS 60665-94-3
:Pentanoic acid, 3-hydroxy-2-methyl-, methyl ester
Description:
Pentanoic acid, 3-hydroxy-2-methyl-, methyl ester, also known as methyl 3-hydroxy-2-methylpentanoate, is an ester derived from pentanoic acid and methanol. This compound features a five-carbon chain with a hydroxyl group and a methyl group on the second and third carbons, respectively. It is a colorless to pale yellow liquid with a characteristic fruity odor. The presence of the hydroxyl group contributes to its solubility in polar solvents, while the ester functional group influences its reactivity and volatility. Pentanoic acid derivatives are often used in the synthesis of various pharmaceuticals, fragrances, and flavoring agents. The compound's molecular structure allows for hydrogen bonding, which can affect its boiling point and solubility in water. Additionally, it may exhibit moderate toxicity and should be handled with care in laboratory settings. As with many esters, it can undergo hydrolysis in the presence of water, reverting to its acid and alcohol components.
Formula:C7H14O3
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Found 1 products.
Methyl 3-hydroxy-2-methylpentanoate
CAS:<p>Methyl 3-hydroxy-2-methylpentanoate is a chemical compound that belongs to the group of alkenoic esters. It is an intermediate in the Baylis-Hillman reaction, which is a chemoenzymatic synthesis used to produce acrylates. Methyl 3-hydroxy-2-methylpentanoate can also be isolated as a byproduct of the weevil, where it was found in the male genitalia. The optical rotation of methyl 3-hydroxy-2-methylpentanoate has been determined to be (+) and it has a molecular weight of 150.</p>Formula:C7H14O3Purity:Min. 95%Molecular weight:146.18 g/mol
