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ChemicalBook--->CAS DataBase List--->684270-46-0

684270-46-0

684270-46-0 Structure

684270-46-0 Structure
IdentificationBack 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 PropertiesBack 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 activity]

[α]/D -10.0±1.0°, c = 1 in DMF
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2924297099
Hazard InformationBack 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).

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