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AI65685

98545-64-3 | Methyl 4-amino-2-bromobenzoate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $9.00 $6.00 -   +
250mg 98% in stock $10.00 $7.00 -   +
1g 98% in stock $18.00 $13.00 -   +
5g 98% in stock $39.00 $28.00 -   +
10g 98% in stock $65.00 $46.00 -   +
25g 98% in stock $114.00 $80.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI65685
Chemical Name: Methyl 4-amino-2-bromobenzoate
CAS Number: 98545-64-3
Molecular Formula: C8H8BrNO2
Molecular Weight: 230.05862000000002
MDL Number: MFCD00859376
SMILES: COC(=O)c1ccc(cc1Br)N

 

Computed Properties
Complexity: 174  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.8  

 

 

Upstream Synthesis Route
  • Methyl 4-amino-2-bromobenzoate is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This compound serves as an important building block in the creation of various pharmaceuticals, agrochemicals, and dyes. Its structure allows for easy modification and functionalization, making it a valuable intermediate in the synthesis of more complex organic molecules.In chemical synthesis, Methyl 4-amino-2-bromobenzoate can undergo a variety of reactions such as acylation, amidation, and condensation to introduce different functional groups into the molecule. These reactions enable chemists to tailor the compound for specific applications by adjusting its chemical and physical properties.Additionally, the presence of both an amino and a bromo group in Methyl 4-amino-2-bromobenzoate offers opportunities for further derivatization through substitution reactions, opening up a wide range of possibilities for creating new compounds with diverse functionalities. Its strategic placement of functional groups makes it a valuable tool for the synthesis of complex organic molecules with precise control over regioselectivity and stereochemistry.
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