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

Description tert-Butyl (S)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate (CAS No. 1375908-92-1) is a high-purity chiral compound with the molecular formula C22H34N2O6. This specialty chemical is an ester derivative featuring a tert-butyl group and a reactive 4-nitrobenzoate moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. The compound’s stereochemistry, defined by the (S)-configuration at the 2-position, ensures enantioselective utility in asymmetric synthesis. With a molecular weight of 422.52 g/mol, it is supplied as a crystalline solid with stringent quality controls, including HPLC and NMR validation, to guarantee ??95% purity. Ideal for researchers exploring peptidomimetics, prodrug development, or novel bioactive molecules, this compound…

Description

Description

tert-Butyl (S)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate (CAS No. 1375908-92-1) is a high-purity chiral compound with the molecular formula C22H34N2O6. This specialty chemical is an ester derivative featuring a tert-butyl group and a reactive 4-nitrobenzoate moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. The compound’s stereochemistry, defined by the (S)-configuration at the 2-position, ensures enantioselective utility in asymmetric synthesis. With a molecular weight of 422.52 g/mol, it is supplied as a crystalline solid with stringent quality controls, including HPLC and NMR validation, to guarantee ??95% purity. Ideal for researchers exploring peptidomimetics, prodrug development, or novel bioactive molecules, this compound is packaged under inert conditions to ensure stability and longevity.

  • CAS No: 1375908-92-1
  • Molecular Formula: C22H34N2O6
  • Molecular Weight: 422.5
  • Exact Mass: 422.24168681
  • Monoisotopic Mass: 422.24168681
  • IUPAC Name: tert-butyl (2S)-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 (S)-2-amino-2-methyldec-9-enoate 4-nitrobenzoate

Application

This compound serves as a versatile chiral building block in medicinal chemistry, particularly for the synthesis of enantiomerically pure amino acid derivatives. Its tert-butyl ester group offers excellent protection for carboxylic acids during multi-step synthetic routes, while the 4-nitrobenzoate moiety enables further functionalization. Researchers utilize it in the development of protease inhibitors, peptide analogs, and constrained scaffolds for drug discovery. The terminal alkene group provides a handle for cross-coupling or click chemistry applications.

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