4-(Boc-amino)indole-3-carboxaldehyde is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in the protection of amines. This compound features an aldehyde functional group (-CHO) at the 3-position of the indole ring, which is reactive and can participate in various chemical reactions, such as condensation and reduction. The presence of the Boc group allows for selective reactions while protecting the amine functionality. The compound is typically used in the synthesis of more complex molecules, including pharmaceuticals and biologically active compounds. It is important to handle this substance with care, following appropriate safety protocols, as it may have specific hazards associated with its reactivity and toxicity. The purity of 97% indicates a high level of quality, making it suitable for research and development applications in organic chemistry and medicinal chemistry.

4-(Boc-aMino)indole-3-carboxaldehyde, 97%

885266-77-3: 4-(Boc-amino)indole-3-carboxaldehyde is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in the protection of amines. This compound features an aldehyde functional group (-CHO) at the 3-position of the indole ring, which is reactive and can participate in various chemical reactions, such as condensation and reduction. The presence of the Boc group allows for selective reactions while protecting the amine functionality. The compound is typically used in the synthesis of more complex molecules, including pharmaceuticals and biologically active compounds. It is important to handle this substance with care, following appropriate safety protocols, as it may have specific hazards associated with its reactivity and toxicity. The purity of 97% indicates a high level of quality, making it suitable for research and development applications in organic chemistry and medicinal chemistry.

<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>

CAS 885266-77-3

4-(Boc-aMino)indole-3-carboxaldehyde, 97%

4-(Boc-amino)indole-3-carboxaldehyde, 97%

Ref: 02-H63587

tert-Butyl 3-formyl-1H-indol-4-ylcarbamate

Ref: IN-DA00H1PX