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Atomfair tert-Butyl (R)-2-amino-2-methylhept-6-enoate 4-nitrobenzoate C19H28N2O6
Description tert-Butyl (R)-2-amino-2-methylhept-6-enoate 4-nitrobenzoate (CAS No. 1323987-68-3) is a high-purity chiral compound with the molecular formula C19H28N2O6. This specialized chemical is designed for advanced research applications, particularly in asymmetric synthesis and pharmaceutical development. The compound features a tert-butyl ester group, an amino functionality, and a 4-nitrobenzoate counterion, making it a valuable intermediate for the preparation of enantiomerically pure compounds. With a well-defined stereocenter at the (R)-2-position, this product is ideal for studies requiring precise chiral control. Supplied as a solid with verified purity, it is suitable for use in organic synthesis, medicinal chemistry, and catalyst development. Store under inert conditions…
Description
Description
tert-Butyl (R)-2-amino-2-methylhept-6-enoate 4-nitrobenzoate (CAS No. 1323987-68-3) is a high-purity chiral compound with the molecular formula C19H28N2O6. This specialized chemical is designed for advanced research applications, particularly in asymmetric synthesis and pharmaceutical development. The compound features a tert-butyl ester group, an amino functionality, and a 4-nitrobenzoate counterion, making it a valuable intermediate for the preparation of enantiomerically pure compounds. With a well-defined stereocenter at the (R)-2-position, this product is ideal for studies requiring precise chiral control. Supplied as a solid with verified purity, it is suitable for use in organic synthesis, medicinal chemistry, and catalyst development. Store under inert conditions at recommended temperatures to ensure stability.
- CAS No: 1323987-68-3
- Molecular Formula: C19H28N2O6
- Molecular Weight: 380.4
- Exact Mass: 380.19473662
- Monoisotopic Mass: 380.19473662
- IUPAC Name: tert-butyl (2R)-2-amino-2-methylhept-6-enoate;4-nitrobenzoic acid
- SMILES: C[C@@](CCCC=C)(C(=O)OC(C)(C)C)N.C1=CC(=CC=C1C(=O)O)[N+](=O)[O-]
- Synonyms: tert-Butyl (R)-2-amino-2-methylhept-6-enoate 4-nitrobenzoate
Application
This compound serves as a key chiral building block in the synthesis of enantioselective pharmaceuticals and bioactive molecules. Researchers utilize it in the development of peptidomimetics and constrained amino acid derivatives. The 4-nitrobenzoate salt form enhances crystallinity for improved handling in synthetic applications. Its structural features make it particularly valuable for studying structure-activity relationships in drug discovery programs.
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