| Identification | Back Directory | [Name]
FMOC-D-AHA-OH | [CAS]
1263047-53-5 | [Synonyms]
FMOC-D-AHA-OH
FMoc-D-Dab(N3)-OH
Fmoc-D-Abu(N3)-OH
Fmoc-D-azidohomoalanine
(R)-4-Azido-2-(Fmoc-amino)-butanoic acid
(2R)-4-azido-2-(Fmoc-amino)butanoic acid
Nα-Fmoc-Nγ-Azido-D-2,4-diaminobutyric acid
(9H-Fluoren-9-yl)MethOxy]Carbonyl D-Dab(N3)-OH
Nα-Fmoc-Nγ-Azido-D-2,4-diaminobutyric acid≥ 98% (HPLC)
(2R)-4-Azido-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]butanoic acid | [Molecular Formula]
C19H18N4O4 | [MDL Number]
MFCD13184927 | [MOL File]
1263047-53-5.mol | [Molecular Weight]
366.371 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
Fmoc-D-Aha-OH is a click chemistry reagent containing an azide[1]. Fmoc-D-Aha-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | [References]
[1] Millward SW, et al. Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1. J Am Chem Soc. 2011 Nov 16;133(45):18280- DOI:10.1021/ja2064389 |
|
| Company Name: |
Shanghai GL Peptide Ltd.
|
| Tel: |
+86-21-61263340; 17609490614 13764994101 |
| Website: |
http://www.yuhua99.com/supplier/10480342/ |
| Company Name: |
Alabiotech Inc.
|
| Tel: |
001-619-354-5251 |
| Website: |
www.alabiotech-e.com |
|