CAS 4649-09-6
:2,9-diazabicyclo[4.3.0]nona-2,4,7,10-tetraene-7-carbaldehyde
Description:
2,9-Diazabicyclo[4.3.0]nona-2,4,7,10-tetraene-7-carbaldehyde, with the CAS number 4649-09-6, is a bicyclic compound characterized by its unique structural framework, which includes a bicyclic system and multiple double bonds. This compound features a diazabicyclic structure, indicating the presence of two nitrogen atoms within the bicyclic framework, contributing to its reactivity and potential applications in organic synthesis. The presence of the aldehyde functional group at the 7-position enhances its reactivity, making it a useful intermediate in various chemical reactions, including condensation and addition reactions. The tetraene system provides conjugation, which can influence the compound's electronic properties and stability. Typically, such compounds exhibit interesting optical properties and can participate in photochemical reactions. Additionally, their structural complexity may lead to unique interactions in biological systems, making them of interest in medicinal chemistry. Overall, 2,9-diazabicyclo[4.3.0]nona-2,4,7,10-tetraene-7-carbaldehyde is a versatile compound with potential applications in various fields of chemistry.
Formula:C8H6N2O
Synonyms:- 1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde
- 3-Formyl-7-Azaindole
- 7-Azaindole-3-Carboxaldehyde
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Found 4 products.
7-Azaindole-3-carboxaldehyde
CAS:Formula:C8H6N2OPurity:97%Color and Shape:SolidMolecular weight:146.14607-Azaindole-3-carboxaldehyde
CAS:<p>7-Azaindole-3-carboxaldehyde</p>Purity:97%Molecular weight:146.15g/mol7-Azaindole-3-carboxaldehyde
CAS:Formula:C8H6N2OPurity:97%Color and Shape:SolidMolecular weight:146.1497-Azaindole-3-carboxaldehyde
CAS:<p>7-Azaindole-3-carboxaldehyde is a molecule that belongs to the class of indoles. It has been shown to have cytotoxic activity in vitro against cancer cells and isomers have been identified. 7-Azaindole-3-carboxaldehyde has been investigated for its ability to bind to CB2 receptors, which are located on the surface of immune cells, and may be used as a lead compound for the development of novel anti-cancer drugs. 7-Azaindole-3-carboxaldehyde also binds to chloride ions, which may be important in understanding how it interacts with other compounds or proteins.</p>Formula:C8H6N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:146.15 g/mol



