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Home  > 3-Bromo-2-methoxybenzoic acid

AA04603

101084-39-3 | 3-Bromo-2-methoxybenzoic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $11.00 $8.00 -   +
5g 98% in stock $19.00 $14.00 -   +
10g 98% in stock $33.00 $23.00 -   +
25g 98% in stock $78.00 $55.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA04603
Chemical Name: 3-Bromo-2-methoxybenzoic acid
CAS Number: 101084-39-3
Molecular Formula: C8H7BrO3
Molecular Weight: 231.0434
MDL Number: MFCD00045840
SMILES: COc1c(Br)cccc1C(=O)O
NSC Number: 76704

 

Computed Properties
Complexity: 172  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 3-Bromo-2-methoxybenzoic acid is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. One key application of this compound is as a building block in the synthesis of biologically active molecules and pharmaceuticals. Its bromine and methoxy functional groups make it a valuable intermediate in the preparation of various organic compounds.In organic synthesis, 3-Bromo-2-methoxybenzoic acid can participate in various reactions such as Suzuki coupling, Heck reaction, and nucleophilic substitution reactions. The bromine atom serves as a crucial site for further functionalization, allowing for the introduction of different substituents to modify the overall chemical structure of the target molecule.Furthermore, the methoxy group provides steric and electronic effects that can influence the reactivity and selectivity of reactions involving the compound. This versatility makes 3-Bromo-2-methoxybenzoic acid a valuable tool for chemists seeking to design and synthesize complex organic molecules with specific biological activities or functional properties.Overall, the application of 3-Bromo-2-methoxybenzoic acid in chemical synthesis offers researchers and chemists a way to access diverse chemical space and explore innovative pathways towards the development of new pharmaceuticals, agrochemicals, and materials.
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