Atomfair tert-Butyl (R)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate C22H34N2O6

Description tert-Butyl (R)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate (CAS No. 1375904-22-5) is a high-purity chiral compound with the molecular formula C22H34N2O6. This specialized chemical features a tert-butyl ester group, an amino acid backbone, and a 4-nitrobenzoate counterion, making it a valuable intermediate for asymmetric synthesis and pharmaceutical research. The compound’s stereochemistry, defined by the (R)-configuration at the 2-position, ensures precise enantioselectivity in synthetic applications. With a molecular weight of 422.52 g/mol, it is supplied as a solid with guaranteed purity (typically ??95% by HPLC) and is rigorously tested for identity (NMR, MS) and impurities (residual solvents, heavy metals). Ideal for use in controlled reactions,…

Description

Description

tert-Butyl (R)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate (CAS No. 1375904-22-5) is a high-purity chiral compound with the molecular formula C22H34N2O6. This specialized chemical features a tert-butyl ester group, an amino acid backbone, and a 4-nitrobenzoate counterion, making it a valuable intermediate for asymmetric synthesis and pharmaceutical research. The compound’s stereochemistry, defined by the (R)-configuration at the 2-position, ensures precise enantioselectivity in synthetic applications. With a molecular weight of 422.52 g/mol, it is supplied as a solid with guaranteed purity (typically ??95% by HPLC) and is rigorously tested for identity (NMR, MS) and impurities (residual solvents, heavy metals). Ideal for use in controlled reactions, this reagent is packaged under inert conditions to ensure stability and shipped with a comprehensive Certificate of Analysis.

  • CAS No: 1375904-22-5
  • Molecular Formula: C22H34N2O6
  • Molecular Weight: 422.5
  • Exact Mass: 422.24168681
  • Monoisotopic Mass: 422.24168681
  • IUPAC Name: tert-butyl (2R)-2-amino-2-methyldec-9-enoate;4-nitrobenzoic acid
  • SMILES: C[C@@](CCCCCCC=C)(C(=O)OC(C)(C)C)N.C1=CC(=CC=C1C(=O)O)[N+](=O)[O-]
  • Synonyms: tert-Butyl (R)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate

Application

This compound serves as a key chiral building block in the synthesis of bioactive molecules, particularly in medicinal chemistry for the development of enantiopure drugs. It is utilized in peptide mimetics and as a precursor for catalysts in asymmetric hydrogenation reactions. Researchers also employ it in the study of enzyme inhibition and receptor binding due to its structurally defined amino acid motif.

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