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Home  > Chemistry  > Organic Building Blocks  > Bromides  > 3-Bromo-1,2-diaminobenzene

AA79483

1575-36-6 | 3-Bromo-1,2-diaminobenzene

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $34.00 $24.00 -   +
5g 95% in stock $50.00 $35.00 -   +
10g 95% in stock $97.00 $68.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA79483
Chemical Name: 3-Bromo-1,2-diaminobenzene
CAS Number: 1575-36-6
Molecular Formula: C6H7BrN2
Molecular Weight: 187.0372
MDL Number: MFCD09842434
SMILES: Nc1c(N)cccc1Br

 

Computed Properties
Complexity: 97.1  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • 3-Bromo-1,2-benzenediamine, also known as 3-Bromo-o-phenylenediamine, is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional properties. In organic chemistry, this compound serves as a key building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates. One common application of 3-Bromo-1,2-benzenediamine is in the preparation of benzimidazoles, which are important heterocyclic compounds with various biological activities. This compound can undergo condensation reactions with aldehydes or ketones to form benzimidazoles through the cyclization process. Benzimidazoles are utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, 3-Bromo-1,2-benzenediamine can participate in coupling reactions to form C-N bonds with various electrophiles. This reactivity makes it a valuable intermediate in the synthesis of azo dyes, which are extensively used in the textile industry for coloring fabrics. The functional groups present in 3-Bromo-1,2-benzenediamine make it an effective coupling partner in the formation of vibrant and stable azo dyes.Furthermore, this compound can also be employed in the construction of polymeric materials through polymerization reactions. By utilizing the amine and bromine functional groups, 3-Bromo-1,2-benzenediamine can be integrated into polymer chains to introduce specific properties or functionalities into the resulting materials. These polymers find applications in various fields, including coatings, adhesives, and biomedical materials.
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