Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
2-Aminobenzeneboronic acid, 96%, Thermo Scientific Chemicals
Have Questions?
Change view
Catalog number L18069.03
also known as L18069-03
Price (USD)/ Each
187.00
-
Quantity:
1 g
Price (USD)/ Each
187.00
2-Aminobenzeneboronic acid, 96%, Thermo Scientific Chemicals
Catalog numberL18069.03
Price (USD)/ Each
187.00
-
Chemical Identifiers
CAS5570-18-3
IUPAC NameN'-[(Z)-(2,5-dimethoxyphenyl)methylidene]-2-[(4-methylphenyl)amino]acetohydrazide
Molecular FormulaC18H21N3O3
InChI KeyPTSWLQVBIWPGOF-JAIQZWGSSA-N
SMILESCOC1=CC=C(OC)C(C=N/NC(=O)CNC2=CC=C(C)C=C2)=C1
View more
Specifications
Specification Sheet
Specification SheetAssay (Aqueous acid-base Titration)≥95.0%
Appearance (Color)White to cream to brown to gray
Proton NMRConforms to structure
FormPowder
Assay (HPLC)≥95.0%
2-Aminobenzeneboronic acid derivative is used in the synthesis of quinolines by reacting with alpha, beta unsaturated ketones. Its hydrochloride derivative is used in the preparation of designed boronate ligands for glucose-selective holographic sensors.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Aminobenzeneboronic acid derivative is used in the synthesis of quinolines by reacting with alpha, beta unsaturated ketones. Its hydrochloride derivative is used in the preparation of designed boronate ligands for glucose-selective holographic sensors.
Notes
Incompatible with oxidizing agents.
2-Aminobenzeneboronic acid derivative is used in the synthesis of quinolines by reacting with alpha, beta unsaturated ketones. Its hydrochloride derivative is used in the preparation of designed boronate ligands for glucose-selective holographic sensors.
Notes
Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Nikitina, V. N.; KOchetkov, I. R.; Karyakina, E. E.; Yatsimirsky, A. K.; Karyakin, A. A. Tuning electropolymerization of boronate-substituted anilines: Fluoride-free synthesis of the advanced affinity transducer. Electrochem. Commun. 2015, 51 121-124.
- Linsenmeier, A. M.; Braje, W. M. Efficient one-pot synthesis of dihydroquinolinones in water at room temperature. Tetrahedron 2015, 71 (38), 6913-6919.