4-Acetyloxy-4-methyl-1-pentanale, identified by its CAS number 110086-93-6, is an organic compound characterized by its functional groups, which include an acetyloxy group and an aldehyde. This compound features a five-carbon chain with a methyl group at the fourth position, contributing to its branched structure. The presence of the acetyloxy group indicates that it can undergo hydrolysis, potentially forming acetic acid and the corresponding alcohol. Its aldehyde functional group suggests reactivity typical of aldehydes, such as oxidation to carboxylic acids or participation in condensation reactions. The compound is likely to be a colorless to pale yellow liquid at room temperature, with a distinctive odor, typical of aldehydes. Its solubility in organic solvents and limited solubility in water reflects its hydrophobic characteristics. Due to its structural features, 4-acetyloxy-4-methyl-1-pentanale may find applications in organic synthesis, flavoring, or fragrance industries, although specific applications would depend on further research into its properties and reactivity.

4-ACETOXY-4-METHYL-1-PENTANAL

110086-93-6: 4-Acetyloxy-4-methyl-1-pentanale, identified by its CAS number 110086-93-6, is an organic compound characterized by its functional groups, which include an acetyloxy group and an aldehyde. This compound features a five-carbon chain with a methyl group at the fourth position, contributing to its branched structure. The presence of the acetyloxy group indicates that it can undergo hydrolysis, potentially forming acetic acid and the corresponding alcohol. Its aldehyde functional group suggests reactivity typical of aldehydes, such as oxidation to carboxylic acids or participation in condensation reactions. The compound is likely to be a colorless to pale yellow liquid at room temperature, with a distinctive odor, typical of aldehydes. Its solubility in organic solvents and limited solubility in water reflects its hydrophobic characteristics. Due to its structural features, 4-acetyloxy-4-methyl-1-pentanale may find applications in organic synthesis, flavoring, or fragrance industries, although specific applications would depend on further research into its properties and reactivity.

CAS 110086-93-6

4-ACETOXY-4-METHYL-1-PENTANAL

2-Methyl-5-oxopentan-2-yl acetate

Ref: IN-DA007VXP

2-Methyl-5-oxopentan-2-yl acetate

Ref: 10-F456666