Pentanal, 5-(phenylmethoxy)-, with the CAS number 78999-24-3, is an organic compound characterized by its structure, which includes a pentanal backbone and a phenylmethoxy substituent. This compound features a five-carbon aldehyde chain, making it part of the aldehyde functional group, which is known for its reactivity due to the presence of the carbonyl group (C=O). The phenylmethoxy group contributes to its aromatic characteristics, potentially influencing its solubility and reactivity. Typically, compounds like this may exhibit moderate volatility and can be soluble in organic solvents. The presence of both aliphatic and aromatic components suggests that it may participate in various chemical reactions, including nucleophilic additions and substitutions. Additionally, such compounds can be of interest in synthetic organic chemistry and may have applications in fragrance, flavoring, or as intermediates in the synthesis of more complex molecules. As with many organic compounds, safety data should be consulted for handling and usage guidelines.

Pentanal, 5-(phenylmethoxy)-

78999-24-3: Pentanal, 5-(phenylmethoxy)-, with the CAS number 78999-24-3, is an organic compound characterized by its structure, which includes a pentanal backbone and a phenylmethoxy substituent. This compound features a five-carbon aldehyde chain, making it part of the aldehyde functional group, which is known for its reactivity due to the presence of the carbonyl group (C=O). The phenylmethoxy group contributes to its aromatic characteristics, potentially influencing its solubility and reactivity. Typically, compounds like this may exhibit moderate volatility and can be soluble in organic solvents. The presence of both aliphatic and aromatic components suggests that it may participate in various chemical reactions, including nucleophilic additions and substitutions. Additionally, such compounds can be of interest in synthetic organic chemistry and may have applications in fragrance, flavoring, or as intermediates in the synthesis of more complex molecules. As with many organic compounds, safety data should be consulted for handling and usage guidelines.

5-(BENZYLOXY)PENTANAL

<p>5-(Benzyloxy)pentanal is a quinoline derivative that inhibits the enzyme reverse transcriptase, which is an extracellular enzyme that synthesizes DNA from RNA. It also inhibits nucleotide synthesis and interacts with other enzymes such as DNA polymerase. 5-(Benzyloxy)pentanal has been shown to inhibit tumor growth by inhibiting the production of cancer-related proteins. The compound was synthesized in a stereoselective manner by reacting piperidine with allyl bromide followed by oxidation to form the corresponding aldehyde. This method was used to produce an enantiomerically pure compound, which exhibits inhibitory activity against HIV-1 integrase.</p>

CAS 78999-24-3

Pentanal, 5-(phenylmethoxy)-

5-(BENZYLOXY)PENTANAL

Ref: 10-F535475

5-(Benzyloxy)pentanal

Ref: 3D-DDA99924