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AX25037

1391528-74-7 | (S)-Methyl 2-amino-2-(4-bromophenyl)acetate hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $251.00 $176.00 -   +
1g 98% in stock $597.00 $418.00 -   +
5g 98% in stock $1,763.00 $1,234.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AX25037
Chemical Name: (S)-Methyl 2-amino-2-(4-bromophenyl)acetate hydrochloride
CAS Number: 1391528-74-7
Molecular Formula: C9H11BrClNO2
Molecular Weight: 280.5461
MDL Number: MFCD12910951
SMILES: COC(=O)[C@H](c1ccc(cc1)Br)N.Cl

 

Computed Properties
Complexity: 179  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • (S)-Methyl 2-amino-2-(4-bromophenyl)acetate hydrochloride is a valuable compound widely utilized in chemical synthesis processes. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and properties make it an essential intermediate for the synthesis of complex organic molecules.In chemical synthesis, (S)-Methyl 2-amino-2-(4-bromophenyl)acetate hydrochloride is often employed as a chiral starting material due to its chirality, allowing for the enantioselective construction of stereocenters in target molecules. Its use can lead to the production of optically active compounds with high purity and selectivity, crucial in the development of pharmaceuticals with desired biological activity.Furthermore, this compound can participate in various chemical transformations such as nucleophilic substitutions, acylation reactions, and cross-coupling reactions, enabling the efficient construction of carbon-carbon and carbon-heteroatom bonds. Its presence in a synthetic pathway can enhance the overall yield, efficiency, and selectivity of the desired product.Overall, the application of (S)-Methyl 2-amino-2-(4-bromophenyl)acetate hydrochloride in chemical synthesis demonstrates its significance as a key reagent for the assembly of structurally diverse and functionally important compounds across different industries.
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