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AC39973

81190-68-3 | 2-Amino-4,6-dibromobenzoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $56.00 $39.00 -   +
1g 97% in stock $121.00 $85.00 -   +
5g 97% in stock $440.00 $308.00 -   +
10g 97% in stock $758.00 $531.00 -   +
25g 97% in stock $1,449.00 $1,015.00 -   +
100g 97% in stock $3,254.00 $2,278.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AC39973
Chemical Name: 2-Amino-4,6-dibromobenzoic acid
CAS Number: 81190-68-3
Molecular Formula: C7H5Br2NO2
Molecular Weight: 294.9281
MDL Number: MFCD12828239
SMILES: Brc1cc(N)c(c(c1)Br)C(=O)O

 

Computed Properties
Complexity: 188  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 2.7  

 

 

Upstream Synthesis Route
  • 2-Amino-4,6-dibromobenzoic acid, a key compound in chemical synthesis, plays a crucial role in various applications within the field of organic chemistry. Its unique molecular structure makes it a valuable building block for the synthesis of complex pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Amino-4,6-dibromobenzoic acid serves as a versatile precursor for the creation of diverse organic compounds. Its amino and carboxylic acid functional groups allow for the modification and functionalization of its structure, enabling the development of novel molecules with tailored properties. By utilizing this compound as a starting material, chemists can access a wide range of derivatives through various chemical transformations such as acylation, amidation, and cyclization reactions.Furthermore, the presence of bromine atoms in 2-Amino-4,6-dibromobenzoic acid confers additional reactivity and diversity to its chemical reactivity. These bromine atoms can participate in substitution reactions, leading to the introduction of new substituents or functional groups into the molecule. This feature enhances the synthetic versatility of 2-Amino-4,6-dibromobenzoic acid and enables the rapid generation of structurally intricate compounds with potential applications in drug discovery, material science, and other chemical fields.
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