Description

(2R)-2-amino-2-methyl-3-(2-nitrophenyl)propanoic acid (CAS: 1241680-73-8) is a high-purity chiral amino acid derivative with a molecular formula of C₁₀H₁₂N₂O₄. This compound features a stereogenic center at the 2-position and a 2-nitrophenyl group, making it a valuable building block for pharmaceutical research and asymmetric synthesis. With a guaranteed purity of >98% and enantiomeric excess (>98%ee), it is ideal for applications requiring precise stereochemical control. The product is supplied as a fine powder, rigorously tested for consistency, and stored under optimal conditions to ensure stability. Suitable for use in peptide synthesis, medicinal chemistry, and biochemical studies.

Properties

• CAS Number: 1241680-73-8
• Complexity: 289
• IUPAC Name: (2R)-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-/m1/s1
• InChI Key: UBTIYKMYANVKMU-SNVBAGLBSA-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: 1241680-73-8, (R)-a-Methyl-2-nitrophenylalanine (>98%, >98%ee), (2R)-2-amino-2-methyl-3-(2-nitrophenyl)propanoic acid, (R)-2-Amino-2-methyl-3-(2-nitrophenyl)propanoic acid, AKOS030213014

This chiral amino acid derivative is widely used in pharmaceutical research for the development of novel therapeutics, particularly in peptide-based drug design. Its stereochemical purity makes it valuable for asymmetric synthesis and catalysis studies. Researchers also utilize it as a precursor in the synthesis of complex bioactive molecules and enzyme inhibitors.

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