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AE09523

10553-14-7 | 7-Nitroindole-3-carboxaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $33.00 $23.00 -   +
5g 95% in stock $72.00 $50.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE09523
Chemical Name: 7-Nitroindole-3-carboxaldehyde
CAS Number: 10553-14-7
Molecular Formula: C9H6N2O3
Molecular Weight: 190.1555
MDL Number: MFCD01074519
SMILES: O=Cc1c[nH]c2c1cccc2N(=O)=O

 

Computed Properties
Complexity: 251  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • 7-Nitroindole-3-carboxyaldehyde is a versatile compound commonly used in chemical synthesis for the development of various organic molecules. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structure and reactivity.In organic synthesis, 7-Nitroindole-3-carboxyaldehyde acts as a valuable precursor in the construction of heterocyclic compounds. Its functional groups enable the formation of complex molecular structures through various reactions such as nucleophilic addition, condensation, and cross-coupling processes. This compound is particularly useful in the production of biologically active compounds where the indole ring system plays a crucial role in the desired pharmacological activity.Additionally, 7-Nitroindole-3-carboxyaldehyde is employed in the synthesis of fluorescent molecules and dyes for analytical and biological imaging applications. Its nitro group can be modulated to introduce specific properties such as fluorescence emission or photophysical characteristics, making it a valuable tool in the development of probes and sensors for various biological systems.Overall, the strategic incorporation of 7-Nitroindole-3-carboxyaldehyde in chemical synthesis facilitates the efficient creation of diverse molecular architectures with tailored functionalities, showcasing its significance in advancing the fields of medicinal chemistry, materials science, and chemical biology.
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