1-Benzyl-1H-indole-5-carbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a benzyl group attached to the nitrogen of the indole and an aldehyde functional group at the 5-position of the indole ring. It typically appears as a yellow to brown solid or liquid, depending on its purity and specific conditions. The presence of the aldehyde group makes it reactive, particularly in condensation reactions and as a potential electrophile in various organic syntheses. Additionally, the indole moiety contributes to its biological activity, as indole derivatives are known for their roles in pharmaceuticals and natural products. The compound may exhibit fluorescence properties, making it useful in certain analytical applications. Its solubility is generally moderate in organic solvents, and it may have specific applications in medicinal chemistry, particularly in the development of new therapeutic agents. Safety data should be consulted for handling and storage, as with all chemical substances.

1-benzyl-1H-indole-5-carbaldehyde

63263-88-7: 1-Benzyl-1H-indole-5-carbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a benzyl group attached to the nitrogen of the indole and an aldehyde functional group at the 5-position of the indole ring. It typically appears as a yellow to brown solid or liquid, depending on its purity and specific conditions. The presence of the aldehyde group makes it reactive, particularly in condensation reactions and as a potential electrophile in various organic syntheses. Additionally, the indole moiety contributes to its biological activity, as indole derivatives are known for their roles in pharmaceuticals and natural products. The compound may exhibit fluorescence properties, making it useful in certain analytical applications. Its solubility is generally moderate in organic solvents, and it may have specific applications in medicinal chemistry, particularly in the development of new therapeutic agents. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 63263-88-7

1-benzyl-1H-indole-5-carbaldehyde

1-Benzylindole-5-carboxaldehyde

Ref: IN-DA00EECH

1-Benzylindole-5-carboxaldehyde

Ref: TR-B279970