Description
(S)-2-Amino-2-methyl-3-(2-nitrophenyl)propanoic acid (CAS: 1241680-71-6) is a high-purity chiral amino acid derivative designed for advanced research and pharmaceutical applications. This compound, with the molecular formula C10H12N2O4, features a stereospecific (S)-configuration and a nitro-substituted phenyl group, making it invaluable for asymmetric synthesis, peptidomimetics, and medicinal chemistry studies. Its rigorous quality control ensures >98% purity (HPLC), ideal for demanding laboratory use. Packaged under inert conditions to guarantee stability, this product is tailored for scientists requiring precision in drug discovery, enzyme inhibition research, and chiral building block development.
Properties
- CAS Number: 1241680-71-6
- Complexity: 289
- IUPAC Name: (2S)-2-amino-2-methyl-3-(2-nitrophenyl)propanoic acid
- InChI: InChI=1S/C10H12N2O4/c1-10(11,9(13)14)6-7-4-2-3-5-8(7)12(15)16/h2-5H,6,11H2,1H3,(H,13,14)/t10-/m0/s1
- InChI Key: UBTIYKMYANVKMU-JTQLQIEISA-N
- Exact Mass: 224.07970687
- Molecular Formula: C10H12N2O4
- Molecular Weight: 224.21
- SMILES: C[C@](CC1=CC=CC=C1[N+](=O)[O-])(C(=O)O)N
- Topological: 109
- Monoisotopic Mass: 224.07970687
- Synonyms: 1241680-71-6, (2S)-2-amino-2-methyl-3-(2-nitrophenyl)propanoic acid, (S)-2-Amino-2-methyl-3-(2-nitrophenyl)propanoic acid, AKOS027339776, F12130, (S)-LFA-METHYL-2-NITROPHENYLALANINE H2O
This compound serves as a key intermediate in the synthesis of chiral pharmaceuticals and bioactive molecules. It is particularly useful in studying enzyme-substrate interactions due to its nitroaromatic moiety. Researchers also employ it in asymmetric catalysis and as a scaffold for peptidomimetic drug design.
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