2. Click Chemistry
  3. Azide
  4. N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine

N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine 

Cat. No.: HY-154835
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N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is an unnatural amino acid. N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine 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.

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N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Chemical Structure

N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Chemical Structure

CAS No. : 1513855-74-7

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Other Forms of N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine:

N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Related Antibodies

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Description

N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is an unnatural amino acid[1]. N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine 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.

Molecular Weight

321.33

Formula

C14H19N5O4
CAS No.
SMILES

N[C@@H](CCCCNC(OCC1=CC=C(N=[N+]=[N-])C=C1)=O)C(O)=O
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Related Classifications

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine1513855-74-7OthersInhibitorinhibitorinhibit

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