Identification | Back 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 |
Hazard Information | Back 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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Company Name: |
Sigma-Aldrich
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Tel: |
021-61415566 800-8193336 |
Website: |
https://www.sigmaaldrich.cn |
Company Name: |
Shanghai GL Peptide Ltd.
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Tel: |
+86-21-61263340; 17609490614 13764994101 |
Website: |
http://www.yuhua99.com/supplier/10480342/ |
Company Name: |
Alabiotech Inc.
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Tel: |
001-619-354-5251 |
Website: |
www.alabiotech-e.com |
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