2098496-96-7

Boc-D-Aza-OH CHA Chemical Structure
2098496-96-7

Chemical Structure

Boc-D-Aza-OH CHA

  • CAS No.: 2098496-96-7
  • Formula:C14H27N5O4
  • Molecular Weight:329.40

IUPAC Name: perfluorophenyl (((9H-fluoren-9-yl)methoxy)carbonyl)-D-methioninate

InChIKey: YDTIDHZIISJNBU-NUBCRITNSA-N

SMILES: CC(C)(C)OC(=O)N[C@H](CN=[N+]=[N-])C(=O)O.C1CCC(CC1)N

Biological Activity: Boc-D-Aza-OH (CHA) is a click chemistry reagent. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity[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.

Cat. No. Product Name Purity Description Pricing
HY-W419403
Boc-D-Aza-OH CHA Boc-D-Aza-OH (CHA) is a click chemistry reagent. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity. 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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