Fmoc-L-Tyr(2-azidoethyl)-OH

Modify Date: 2024-09-17 11:33:51

Fmoc-L-Tyr(2-azidoethyl)-OH structure	Common Name	Fmoc-L-Tyr(2-azidoethyl)-OH
	CAS Number	1454816-10-4	Molecular Weight	472.49
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₂₆H₂₄N₄O₅	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of Fmoc-L-Tyr(2-azidoethyl)-OH

Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters[1].

Name	Fmoc-L-Tyr(2-azidoethyl)-OH

Description	Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Jolita Seckute, et al. Rapid oligonucleotide-templated fluorogenic tetrazine ligations. Nucleic Acids Res. 2013 Aug;41(15):e148.

Molecular Formula	C₂₆H₂₄N₄O₅
Molecular Weight	472.49

Fmoc-L-Tyr(2-azidoethyl)-OH

Use of Fmoc-L-Tyr(2-azidoethyl)-OH

Names

Fmoc-L-Tyr(2-azidoethyl)-OH Biological Activity

Chemical & Physical Properties