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Cat. No.: HY-151663

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Fmoc-Abu(3-N3) (2R,3R)

Name: Fmoc-Abu(3-N3) (2R,3R)
Brand: MedChemExpress
SKU: HY-151663
Availability: PreOrder

(Synonyms: Fmoc-Abu(3-N3)-OH (2R,3R))

Fmoc-Abu(3-N3) (Fmoc-Abu(3-N3)-OH) (2R,3R) is a click chemistry reagent containing an azide group. Fmoc-Abu(3-N3) (2R,3R) can be used for the research of various biochemical. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.

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CAS No.: 1229394-75-5
Formula: C₁₉H₁₈N₄O₄
Molecular Weight:366.37

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (268 KB)

Fmoc-Abu(3-N3) (2R,3R) Chemical Structure

CAS No.: 1229394-75-5

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Description

Fmoc-Abu(3-N3) (Fmoc-Abu(3-N3)-OH) (2R,3R) is a click chemistry reagent containing an azide group. Fmoc-Abu(3-N3) (2R,3R) can be used for the research of various biochemical^[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.

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Chemical Information

CAS No. 1229394-75-5
Molecular Weight 366.37
Formula C₁₉H₁₈N₄O₄
SMILES

[N-]=[N+]=N[C@H](C)[C@H](C(O)=O)NC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O
Synonyms

Fmoc-Abu(3-N3)-OH (2R,3R)
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

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Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (268 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Izzo, et al. Solid-phase synthesis of aza-kahalalide F analogues: (2R,3R)-2-amino-3-azidobutanoic acid as precursor of the aza-threonine. European Journal of Organic Chemistry. Issue: 13. Pages: 2536-2543, S2536/1-S2536/23. Journal.

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How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Fmoc-Abu(3-N3) (2R,3R)

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