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ChemicalBook--->CAS DataBase List--->263847-08-1

263847-08-1

263847-08-1 Structure

263847-08-1 Structure
IdentificationBack Directory
[Name]

(2S,4S)-1-fMoc-4-azidopyrrolidine-2-carboxylic acid
[CAS]

263847-08-1
[Synonyms]

Fmoc-Pro(4-N3)-OH
Fmoc-cis-N3-Pro-OH
cis-FMoc-Pro(4-N3)-OH
FMOC-4-AZIDOPROLINE 1 G
Fmoc-2S,4S-azidoproline
Fmoc-cis-Pro(4-azido)-OH
Fmoc-L-cis-4-azidoproline
FMOC-4-AZIDOPROLINE 250 MG
Fmoc-L-Pro(4-N3)-OH (2S,4S)
cis-4-Azido-N-Fmoc-L-proline
(2S,4S)-1-fMoc-4-azidopyrrolidine-2-carboxylic acid
(2S,4S)-Fmoc-4-azido-pyrrolidine-2-carboxylic acid≥ 99% (HPLC)
Fmoc-cis-N3-Pro-OH,cis-4-Azido-N-Fmoc-L-proline,Fmoc-L-cis-4-azidoproline
(2S,4S)-4-Azido-1,2-pyrrolidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester
(2S,4S)-4-azido-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}pyrrolidine-2-carboxylic acid
[Molecular Formula]

C20H18N4O4
[MDL Number]

MFCD04115792
[MOL File]

263847-08-1.mol
[Molecular Weight]

378.381
Chemical PropertiesBack Directory
[storage temp. ]

Store at -15°C to -25°C.
[form ]

Solid
[color ]

White to off-white
Safety DataBack Directory
[HS Code ]

2933998090
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder
[Uses]

peptide synthesis
[General Description]

A useful tool for the synthesis of branched, side-chain modified and cyclic peptides by Fmoc SPPS. The side-chain azido group is completely stable to piperidine and TFA, but can be readily converted to an amine on the solid phase or in solution by reduction with thiols [1] or phosphines [2, 3].
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
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