ChemicalBook--->CAS DataBase List--->1097192-04-5

1097192-04-5

1097192-04-5 Structure

1097192-04-5 Structure
IdentificationBack Directory
[Name]

Fmoc-δ-azido-Nva-OH
[CAS]

1097192-04-5
[Synonyms]

FMoc-Orn(N2)-OH
Fmoc-L-Orn(N3)-OH
Fmoc-δ-azido-Nva-OH
FMoc-d-azido-Nva-OH
FMoc-L-azidoornithine
Fmoc-δ-azidonorvaline
FMOC-L-DELTA-AZIDOORNITHINE
Ná-Fmoc-Nδ-azido-L-ornithine
Fmoc-δ-azido-Nva-OH USP/EP/BP
(2S)-Fmoc-5-azidopentanoicacid
(2S)-N-FMoc-5-azido--Pentenoic acid
(S)-5-Azido-2-(FMoc-aMino)pentanoic acid
(S)-2-(Fmoc-amino)-5-azidopentanoic Acid
(9H-Fluoren-9-yl)MethOxy]Carbonyl L-Orn(N3)-OH
5-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norvaline
(S)-2-(9-Fluorenylmethyloxycarbonylamino)-5-azidopentanoic acid
(2S)-5-azido-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoicaci
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-azidopentanoic acid
(2S)-5-azido-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoic acid
[Molecular Formula]

C20H20N4O4
[MDL Number]

MFCD11052921
[MOL File]

1097192-04-5.mol
[Molecular Weight]

380.397
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[form ]

crystalline powder
[color ]

White
[Optical Rotation]

[α]/D 3.5±0.3°, c = 1 in ethyl acetate
[Major Application]

peptide synthesis
[InChI]

1S/C20H20N4O4/c21-24-22-11-5-10-18(19(25)26)23-20(27)28-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,23,27)(H,25,26)/t18-/m0/s1
[InChIKey]

TVPIDQLSARDIPX-SFHVURJKSA-N
[SMILES]

OC(=O)[C@H](CCCN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2929 90 00
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

(S)?-?Fmoc-?2-?amino-?5-?azido-?pentanoic Acid is a chiral reagent used in preparing macrocyclic constraints in peptides (peptide stapling) which is an important tool in medicinal peptide chemistry. in addition, (S)?-?Fmoc-?2-?amino-?5-?azido-?pentanoic Acid has been used in the synthesis of clicked peptides.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
reaction type: click chemistry
Spectrum DetailBack Directory
[Spectrum Detail]

Fmoc-δ-azido-Nva-OH(1097192-04-5)1HNMR
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