73259-81-1
73259-81-1
Chemical Structure
Boc-L-Dap-OH
- CAS No.: 73259-81-1
- Formula:C8H16N2O4
- Molecular Weight:204.23
IUPAC Name: (S)-3-amino-2-((tert-butoxycarbonyl)amino)propanoic acid
InChIKey: KRJLRVZLNABMAT-YFKPBYRVSA-N
SMILES: O=C(O)[C@H](CN)NC(OC(C)(C)C)=O
Biological Activity: Boc-L-Dap-OH is a Boc-protected derivative of L-2,3-diaminopropionic acid. Boc-L-Dap-OH is an important chiral amino acid derivative. Boc-L-Dap-OH can be generated via the Hofmann rearrangement of Boc-L-asparagine. Boc-L-Dap-OH serves as a starting material for the preparation of BIM analogs[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Boc-L-Dap-OH | 98.0% | Boc-L-Dap-OH is a Boc-protected derivative of L-2,3-diaminopropionic acid. Boc-L-Dap-OH is an important chiral amino acid derivative. Boc-L-Dap-OH can be generated via the Hofmann rearrangement of Boc-L-asparagine. Boc-L-Dap-OH serves as a starting material for the preparation of BIM analogs. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Küppers J, et al. Tetrahydroimidazo [1, 2‐a] pyrazine Derivatives: Synthesis and Evaluation as Gαq‐Protein Ligands[J]. Chemistry–A European Journal, 2020, 26(55): 12615-12623.
- [2]. Ohyoshi T, et al. Total synthesis of (−)-aplaminal by Buchwald–Hartwig cross-coupling of an aminal[J]. New Journal of Chemistry, 2019, 43(47): 18442-18444.
Keywords
