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AA02510

100487-82-9 | Methyl 2-(4-bromo-2-nitrophenyl)acetate

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $31.00 $22.00 -   +
5g 97% in stock $122.00 $86.00 -   +
10g 97% in stock $227.00 $159.00 -   +
25g 97% in stock $511.00 $358.00 -   +
100g 97% in stock $1,536.00 $1,075.00 -   +

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Description
Catalog Number: AA02510
Chemical Name: Methyl 2-(4-bromo-2-nitrophenyl)acetate
CAS Number: 100487-82-9
Molecular Formula: C9H8BrNO4
Molecular Weight: 274.0681
MDL Number: MFCD09027267
SMILES: COC(=O)Cc1ccc(cc1[N+](=O)[O-])Br

 

Computed Properties
Complexity: 253  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 3  
XLogP3: 2.2  

 

 

Upstream Synthesis Route
  • Methyl 2-(4-bromo-2-nitrophenyl)acetate, a versatile chemical compound, plays a crucial role in chemical synthesis as a key building block. Its unique structure containing a bromo and nitro functional group enables it to participate in various synthetic reactions, making it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals.In organic synthesis, Methyl 2-(4-bromo-2-nitrophenyl)acetate serves as a significant intermediate for the preparation of complex molecules. It can undergo substitution reactions, such as nucleophilic aromatic substitution, to introduce diverse functional groups onto the phenyl ring. This flexibility allows chemists to tailor the molecule's properties for specific applications.Furthermore, the presence of the ester group in Methyl 2-(4-bromo-2-nitrophenyl)acetate offers opportunities for further functionalization through esterification or hydrolysis reactions. The acetate moiety can be transformed into different functional groups, expanding the compound's synthetic versatility.Overall, Methyl 2-(4-bromo-2-nitrophenyl)acetate's role in chemical synthesis lies in its ability to act as a versatile precursor for the construction of complex molecules with tailored properties. Its strategic position in various synthetic pathways makes it a valuable tool for organic chemists striving to develop novel compounds for a range of industries.
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