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Home  > Chemistry  > Organic Building Blocks  > Bromides  > 2,4-Dibromo-5-methoxyaniline

AB43613

35736-52-8 | 2,4-Dibromo-5-methoxyaniline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $10.00 $7.00 -   +
1g 95% in stock $30.00 $21.00 -   +
5g 95% in stock $106.00 $74.00 -   +
100g 95% in stock $1,535.00 $1,074.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB43613
Chemical Name: 2,4-Dibromo-5-methoxyaniline
CAS Number: 35736-52-8
Molecular Formula: C7H7Br2NO
Molecular Weight: 280.9446
MDL Number: MFCD08282833
SMILES: COc1cc(N)c(cc1Br)Br

 

Computed Properties
Complexity: 134  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 2.6  

 

 

Upstream Synthesis Route
  • 2,4-dibromo-5-methoxyaniline is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a vital building block in the creation of various organic molecules due to its functional groups and reactivity. In particular, 2,4-dibromo-5-methoxyaniline is commonly employed in the pharmaceutical industry for the synthesis of novel drug candidates and bioactive compounds.One of the key applications of 2,4-dibromo-5-methoxyaniline is as a precursor in the synthesis of heterocyclic compounds, such as indoles and benzimidazoles. These heterocycles are essential components in the design and development of pharmaceuticals, agrochemicals, and materials science. By leveraging the reactivity of the bromine and methoxy substituents on the aniline ring, chemists can selectively modify the molecule to introduce specific functionalities, enhancing the biological activity or properties of the final product.Furthermore, 2,4-dibromo-5-methoxyaniline plays a crucial role in the construction of complex organic molecules through various coupling reactions, such as Suzuki-Miyaura cross-coupling and Buchwald-Hartwig amination. These synthetic protocols allow for the formation of carbon-carbon and carbon-nitrogen bonds, enabling the incorporation of diverse molecular fragments into a target molecule. This versatility makes 2,4-dibromo-5-methoxyaniline a valuable tool in the arsenal of synthetic chemists for the efficient assembly of structurally intricate compounds with tailored properties.
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