2483829-89-4

L-Azidohomoalanine-1,2,3,4-<sup>13</sup>C<sub>4</sub> hydrochloride Chemical Structure
2483829-89-4

Chemical Structure

L-Azidohomoalanine-1,2,3,4-13C4 hydrochloride

  • CAS No.: 2483829-89-4
  • Formula:13C4H9ClN2 15N2O2
  • Molecular Weight:186.55

IUPAC Name: (S)-2-(amino-15N)-4-(azido)butanoic-1,2,3,4-13C4 acid hydrochloride

InChIKey: MHHYJRIDKLZZEO-PIUPILLASA-N

SMILES: [N-]=[N+]=[15N][13CH2][13CH2][13C@H]([15NH2])[13C](O)=O.Cl

Biological Activity: L-Azidohomoalanine-1,2,3,4-13C4 (hydrochloride) is the 13C- and 15N-labeled L-Azidohomoalanine hydrochloride. L-Azidohomoalanine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]. L-Azidohomoalanine-1,2,3,4-13C4 (hydrochloride) 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.

Cat. No. Product Name Purity Description Pricing
HY-140346AS
L-Azidohomoalanine-1,2,3,4-13C4 hydrochloride L-Azidohomoalanine-1,2,3,4-13C4 (hydrochloride) is the 13C- and 15N-labeled L-Azidohomoalanine hydrochloride. L-Azidohomoalanine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-Azidohomoalanine-1,2,3,4-13C4 (hydrochloride) 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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HY-140346A
L-Azidohomoalanine hydrochloride 99.88% L-Azidohomoalanine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-Azidohomoalanine (hydrochloride) 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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