16348-49-5
Chemical Structure
2-Amino benzamidoxime
Synonym(s): ABAO
- CAS No.: 16348-49-5
- Formula:C7H9N3O
- Molecular Weight:151.17
IUPAC Name: 2-amino-N-hydroxybenzimidamide
InChIKey: CFZHYRNQLHEHJS-UHFFFAOYSA-N
SMILES: N=C(NO)C1=CC=CC=C1N
Biological Activity:
2-Amino benzamidoxime (ABAO) acts as a bioconjugation reagent precursor and a fluorescent probe precursor. 2-Amino benzamidoxime contains an aniline group for imine activation of aldehydes, as well as a nucleophilic group (Nu:) located at the ortho position of the amine, which is responsible for intramolecular cyclization. 2-Amino benzamidoxime reacts with glyoxal at the N-terminus of phage-displayed peptide libraries. Derivatives of 2-Amino benzamidoxime can be used for protein bioconjugation. Derivatives of 2-Amino benzamidoxime serve as fluorescent probes[1].\n
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Amino benzamidoxime | 99.85% | 2-Amino benzamidoxime (ABAO) acts as a bioconjugation reagent precursor and a fluorescent probe precursor. 2-Amino benzamidoxime contains an aniline group for imine activation of aldehydes, as well as a nucleophilic group (Nu:) located at the ortho position of the amine, which is responsible for intramolecular cyclization. 2-Amino benzamidoxime reacts with glyoxal at the N-terminus of phage-displayed peptide libraries. Derivatives of 2-Amino benzamidoxime can be used for protein bioconjugation. Derivatives of 2-Amino benzamidoxime serve as fluorescent probes.\n |
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Keywords
