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

Cat. No.: HY-151693A: Fiche technique Instruction de manipulation
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H-L-Tyr(2-azidoethyl)-OH is a unnatural Tyrosine derivative. H-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. 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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H-L-Tyr(2-azidoethyl)-OH Chemical Structure

CAS No. : 1570523-47-5

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Other In-stock Forms of H-L-Tyr(2-azidoethyl)-OH:

H-L-Tyr(2-azidoethyl)-OH hydrochloride

Other Forms of H-L-Tyr(2-azidoethyl)-OH:

H-L-Tyr(2-azidoethyl)-OH hydrochloride In-stock

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Description	H-L-Tyr(2-azidoethyl)-OH is a unnatural Tyrosine derivative. H-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group^[1]^[2]. 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.
Masse moléculaire	250.25
Formule	C₁₁H₁₄N₄O₃
CAS No.	1570523-47-5
SMILES	OC([C@@H](N)CC1=CC=C(C=C1)OCCN=[N+]=[N-])=O
Livraison	Room temperature in continental US; may vary elsewhere.
Stockage	Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation	Fiche technique (264 KB) Instruction de manipulation (2659 KB)
Références	[1]. Tookmanian EM, et al. Azidoethoxyphenylalanine as a Vibrational Reporter and Click Chemistry Partner in Proteins. Chemistry. 2015 Dec 21;21(52):19096-103. [Content Brief] [2]. Maza JC, et al. Synthesis and Incorporation of Unnatural Amino Acids To Probe and Optimize Protein Bioconjugations. Bioconjug Chem. 2015 Sep 16;26(9):1884-9. [Content Brief]