76387-70-7
Chemical Structure
Boc-D-2,3-diaminopropionic acid
Synonym(s): N-t-Boc-amino-D-alanine; Boc-D-Dap-OH
- CAS No.: 76387-70-7
- Formula:C8H16N2O4
- Molecular Weight:204.23
IUPAC Name: (R)-3-amino-2-((tert-butoxycarbonyl)amino)propanoic acid
InChIKey: KRJLRVZLNABMAT-RXMQYKEDSA-N
SMILES: O=C(O)[C@@H](CN)NC(OC(C)(C)C)=O
Biological Activity: Boc-D-2,3-diaminopropionic acid (N-t-Boc-amino-D-alanine; Boc-D-Dap-OH) is a Boc-protected D-diamino acid building block that serves as a precursor for the synthesis of fluorescent carbon dots and fluorescent D-amino acid probes (such as HADA and NADA), and can be used in amide coupling reactions. Boc-D-2,3-diaminopropionic acid is applicable to fluorescent probe development and chemical biology research[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Boc-D-2,3-diaminopropionic acid | 97.0% | Boc-D-2,3-diaminopropionic acid (N-t-Boc-amino-D-alanine; Boc-D-Dap-OH) is a Boc-protected D-diamino acid building block that serves as a precursor for the synthesis of fluorescent carbon dots and fluorescent D-amino acid probes (such as HADA and NADA), and can be used in amide coupling reactions. Boc-D-2,3-diaminopropionic acid is applicable to fluorescent probe development and chemical biology research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Wang Q, et al. Carbon Dots: A Versatile Platform for Cu Detection, Anti-Counterfeiting, and Bioimaging. Molecules (Basel, Switzerland). 2024 Sep 05;29(17):4211.
- [2]. Cambray S, et al. Fluorogenic diazaborine formation of semicarbazide with designed coumarin derivatives. Chemical communications (Cambridge, England). 2017 Nov 21;53(93):12532-12535.
- [3]. Tsui HT, et al. Pbp2x localizes separately from Pbp2b and other peptidoglycan synthesis proteins during later stages of cell division of Streptococcus pneumoniae D39. Molecular microbiology. 2014 Oct;94(1):21-40.
- [4]. Zhao F, et al. Derivatives of ()-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific Activity. Journal of medicinal chemistry. 2022 Jan 13;65(1):734-746. [Content Brief]
