1807631-13-5
Chemical Structure
N3-D-Dap(Fmoc)-OH
- CAS No.: 1807631-13-5
- Formula:C18H16N4O4
- Molecular Weight:352.34
IUPAC Name: 3,6-bis(5-bromothiophen-2-yl)-2,5-didodecyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
InChIKey: QJCYGENXFLOOKP-MRXNPFEDSA-N
SMILES: [N-]=[N+]=N[C@@H](C(O)=O)CNC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O
Biological Activity: N3-D-Dap(Fmoc)-OH is a click chemistry reagent. N3-D-Dap(Fmoc)-OH can be used as a component for coupling by click reaction and as an orthogonally protected diaminocarboxylic acid derivative. N3-D-Dap(Fmoc)-OH contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. N3-D-Dap(Fmoc)-OH can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N3-D-Dap(Fmoc)-OH | 99.96% | N3-D-Dap(Fmoc)-OH is a click chemistry reagent. N3-D-Dap(Fmoc)-OH can be used as a component for coupling by click reaction and as an orthogonally protected diaminocarboxylic acid derivative. N3-D-Dap(Fmoc)-OH contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. N3-D-Dap(Fmoc)-OH can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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Keywords
