4-Octenal, 4,6-dimethyl-, (E)-, with the CAS number 88056-89-7, is an organic compound characterized by its unsaturated aldehyde structure. It features a long carbon chain with a double bond between the fourth and fifth carbon atoms, and a carbonyl group at the first position, which is typical of aldehydes. The "(E)" designation indicates that the double bond has a specific geometric configuration, where the higher priority substituents on either side of the double bond are on opposite sides, contributing to its overall stability and reactivity. This compound is likely to be a colorless to pale yellow liquid with a distinctive odor, typical of many aldehydes. It is soluble in organic solvents and may exhibit moderate volatility. 4-Octenal, 4,6-dimethyl-, (E)- is used in various applications, including as a flavoring agent and in the synthesis of other organic compounds. Its reactivity is influenced by the presence of the double bond and the aldehyde functional group, making it a valuable intermediate in organic synthesis.

4-Octenal, 4,6-dimethyl-, (E)-

88056-89-7: 4-Octenal, 4,6-dimethyl-, (E)-, with the CAS number 88056-89-7, is an organic compound characterized by its unsaturated aldehyde structure. It features a long carbon chain with a double bond between the fourth and fifth carbon atoms, and a carbonyl group at the first position, which is typical of aldehydes. The "(E)" designation indicates that the double bond has a specific geometric configuration, where the higher priority substituents on either side of the double bond are on opposite sides, contributing to its overall stability and reactivity. This compound is likely to be a colorless to pale yellow liquid with a distinctive odor, typical of many aldehydes. It is soluble in organic solvents and may exhibit moderate volatility. 4-Octenal, 4,6-dimethyl-, (E)- is used in various applications, including as a flavoring agent and in the synthesis of other organic compounds. Its reactivity is influenced by the presence of the double bond and the aldehyde functional group, making it a valuable intermediate in organic synthesis.

CAS 88056-89-7

4-Octenal, 4,6-dimethyl-, (E)-