| Identification | Back Directory | [Name]
(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID | [CAS]
684270-46-0 | [Synonyms]
FMOC-AZA-OH
Fmoc-L-Aza-OH
Fmoc-Ala(N3)-OH
Fmoc-L-Dap(N3)-OH
Fmoc-L-azidoalanin
FMoc-β-azido-Ala-OH
FMOC-L-AZIDOALANINE
FMoc-β-azidoalanine
Fmoc-L-Aza-OH (solv.)
FMOC-3-azido-L-alanine
Fmoc-beta-azido-Ala-OH
3-azido-N-Fmoc-L-ala-OH
FMOC-L-BETA-AZIDOALANINE
3-Azido-N-Fmoc-L-alanine
FMoc-beta-azido-Ala-OH >=98.0% (HPLC)
2-(S)-Fmoc-amino-3-azidopropanoic acid
(9H-Fluoren-9-yl)MethOxy]Carbonyl Dap(N3)-OH
Nα-Fmoc-Nβ-Azido-L-2,3-diaminopropionic acid
3-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine
(2S)-3-azido-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoicaci
(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID
(2S)-3-azido-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
Nα-Fmoc-Nβ-Azido-L-2,3-diaminopropionic acidSolvate with DIPE≥ 99% (HPLC)
(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID USP/EP/BP | [Molecular Formula]
C18H16N4O4 | [MDL Number]
MFCD11052919 | [MOL File]
684270-46-0.mol | [Molecular Weight]
352.35 |
| Chemical Properties | Back Directory | [Melting point ]
>155 (dec.) | [storage temp. ]
2-8°C | [solubility ]
DMF (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White | [Optical Rotation]
[α]/D -10.0±1.0°, c = 1 in DMF | [Major Application]
peptide synthesis | [InChI]
InChI=1/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/s3 | [InChIKey]
ZITYCUDVCWLHPG-QEIABERDNA-N | [SMILES]
C(C1C2=CC=CC=C2C2=CC=CC=C12)OC(=O)N[C@H](C(=O)O)CN=[N+]=[N-] |&1:18,r| |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white crystalline powder | [Uses]
Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.
It can be used in:
- Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).
- Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.
- Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).
| [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis
reaction type: click chemistry |
|
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Energy Chemical
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