Boc-D-2,3-diaminopropionic acid
Based on 1 Customer Validation
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.
For research use only. We do not sell to patients.
- Purity : 97.0%
- CAS No.: 76387-70-7
- Formula: C8H16N2O4
- Molecular Weight:204.23
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Storage:
Store at room temperature 3 years.
In solvent -80°C, 2 years , -20°C, 1 year
Biological Activity
Description
In Vitro
Boc-D-2,3-diaminopropionic acid (N-t-Boc-amino-D-alanine; Boc-D-Dap-OH) (1.0 mmol; overnight) is a building block that undergoes EDCI/HOBt-mediated amide coupling with 5-substituted furan-2-carboxylic acids to afford Boc-protected intermediates for the synthesis of NMDA receptor glycine site agonist analogs[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 76387-70-7
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Appearance Solid
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Molecular Weight 204.23
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Formula C8H16N2O4
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Color White to off-white
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Synonyms
N-t-Boc-amino-D-alanine; Boc-D-Dap-OH
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Store at room temperature 3 years
In solvent -80°C 2 years -20°C 1 year
Purity & Documentation
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Data Sheet (268 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- Boc-D-2,3-diaminopropionic acid
- 76387-70-7
- N-t-Boc-amino-D-alanine
- Boc-D-Dap-OH
- Amino Acid Derivatives
- NMDA receptor glycine site agonist analogues
- hydrothermal reaction
- diaminomaleonitrile
- semicarbazide derivative
- NADA
- fluorescent D-amino acid probe synthesis
- amide coupling reactions
- fluorescent carbon dot
- HADA
- Boc-protected D-diamino acid synthetic building block
- Inhibitor
- inhibitor
- inhibit