2165877-62-1
Chemical Structure
N3-D-Orn(Boc)-OH
- CAS No.: 2165877-62-1
- Formula:C10H18N4O4
- Molecular Weight:258.27
IUPAC Name: (R)-2-azido-5-((tert-butoxycarbonyl)amino)pentanoic acid
InChIKey: DPHZPVOCMJNGEU-SSDOTTSWSA-N
SMILES: CC(C)(C)OC(NCCC[C@H](C(O)=O)N=[N+]=[N-])=O
Biological Activity: N3-D-Orn(Boc)-OH is a Boc-protected pentanoic amino acid derivative, can be used as a click chemistry reagent and has been used to synthesis antibody-drug conjugates (ADC)[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
N3-D-Orn(Boc)-OH | N3-D-Orn(Boc)-OH is a Boc-protected pentanoic amino acid derivative, can be used as a click chemistry reagent and has been used to synthesis antibody-drug conjugates (ADC). It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
