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AA06534

101682-68-2 | 3-Bromo-4-nitrobenzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $60.00 $42.00 -   +
1g 98% in stock $72.00 $51.00 -   +
5g 98% in stock $245.00 $172.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA06534
Chemical Name: 3-Bromo-4-nitrobenzaldehyde
CAS Number: 101682-68-2
Molecular Formula: C7H4BrNO3
Molecular Weight: 230.01555999999997
MDL Number: MFCD00968939
SMILES: O=Cc1ccc(c(c1)Br)[N+](=O)[O-]

 

Computed Properties
Complexity: 192  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 1  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • 3-Bromo-4-nitrobenzaldehyde is a versatile compound that finds wide application in chemical synthesis due to its unique properties and reactivity. This compound is commonly used as a building block in the synthesis of various organic compounds, especially in the pharmaceutical and agrochemical industries. Its strategic placement of a bromine and nitro group on the benzene ring imparts specific characteristics that are crucial in the design and preparation of target molecules.In organic synthesis, 3-Bromo-4-nitrobenzaldehyde serves as a key intermediate in the preparation of pharmaceuticals, dyes, and other complex organic molecules. Its ability to undergo diverse chemical reactions, such as nucleophilic substitutions, condensations, and reductions, allows for the efficient construction of intricate molecular structures. Furthermore, the presence of electron-withdrawing groups in its structure can facilitate the synthesis of biologically active compounds by influencing the pharmacological properties of the final products.Additionally, the reactivity of 3-Bromo-4-nitrobenzaldehyde can be harnessed in the preparation of functionalized aromatic compounds and heterocyclic derivatives, contributing to the advancement of medicinal chemistry and materials science. Its role in organic transformations highlights its importance as a valuable synthetic building block for the development of new molecules with potential industrial applications.
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