logo
Home  > (R)-4-(1-Aminoethyl)benzoic acid

AB55674

1108683-66-4 | (R)-4-(1-Aminoethyl)benzoic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $145.00 $101.00 -   +
1g 98% in stock $275.00 $192.00 -   +
5g 98% in stock $713.00 $499.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB55674
Chemical Name: (R)-4-(1-Aminoethyl)benzoic acid
CAS Number: 1108683-66-4
Molecular Formula: C9H11NO2
Molecular Weight: 165.1891
MDL Number: MFCD06761798
SMILES: C[C@H](c1ccc(cc1)C(=O)O)N

 

Upstream Synthesis Route
  • The (R)-4-(1-Aminoethyl)benzoic acid, commonly known as $name$, serves as a versatile building block in chemical synthesis. Due to its strategic placement of a chiral center and an amino group on the benzene ring, this compound plays a crucial role in the creation of complex molecules with specific stereochemistry and functionality. In chemical synthesis, (R)-4-(1-Aminoethyl)benzoic acid is often utilized as a key intermediate for the production of various pharmaceuticals, agrochemicals, and materials. Its amino group can undergo diverse transformations, such as acylation, alkylation, and condensation reactions, allowing for the introduction of different functional groups. This enables chemists to tailor the structure and properties of the resulting molecules for specific applications.Moreover, the chiral nature of (R)-4-(1-Aminoethyl)benzoic acid makes it particularly valuable in asymmetric synthesis. By leveraging the inherent chirality of this compound, researchers can access enantiomerically pure compounds, which are essential in drug development and other fields where stereochemistry plays a critical role.Overall, (R)-4-(1-Aminoethyl)benzoic acid stands as a valuable tool in the hands of synthetic chemists, enabling the construction of intricate and diverse molecular architectures for a wide range of industrial and scientific purposes.
FEATURED PRODUCTS