AB61397
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $11.00 | $8.00 | - + | |
1g | 98% | in stock | $43.00 | $31.00 | - + | |
5g | 98% | in stock | $214.00 | $150.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB61397 |
Chemical Name: | 2-Bromo-4-nitrobenzaldehyde |
CAS Number: | 5274-71-5 |
Molecular Formula: | C7H4BrNO3 |
Molecular Weight: | 230.0156 |
MDL Number: | MFCD08753661 |
SMILES: | O=Cc1ccc(cc1Br)[N+](=O)[O-] |
Complexity: | 192 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 1 |
XLogP3: | 1.9 |
2-Bromo-4-nitrobenzaldehyde is a versatile compound widely utilized in chemical synthesis for its unique properties. In organic chemistry, this compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its reactive nature, 2-Bromo-4-nitrobenzaldehyde is commonly used as a precursor in the synthesis of complex organic molecules through various chemical reactions such as nucleophilic substitution, Suzuki coupling, and Grignard reactions. Its nitro and bromo functional groups make it a valuable reagent for introducing specific chemical functionalities into target molecules. Additionally, the aldehyde group in 2-Bromo-4-nitrobenzaldehyde enables it to participate in aldol condensation reactions, leading to the formation of diverse chemical structures with potential biological activities. Overall, 2-Bromo-4-nitrobenzaldehyde plays a crucial role in modern organic synthesis, facilitating the development of novel compounds with applications across various industries.