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2-Aminobenzeneboronic acid, 96%, Thermo Scientific Chemicals
Catalog number: L18069.06
5 g, Each
Thermo Scientific Chemicals
2-Aminobenzeneboronic acid, 96%, Thermo Scientific Chemicals
Catalog number: L18069.06
5 g, Each
Quantity
Catalog number: L18069.06
also known as L18069-06
Price (USD)
642.00
Each
Quantity
-
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Chemical Identifiers
CAS
5570-18-3
IUPAC Name
N'-[(Z)-(2,5-dimethoxyphenyl)methylidene]-2-[(4-methylphenyl)amino]acetohydrazide
Molecular Formula
C18H21N3O3
InChI Key
PTSWLQVBIWPGOF-JAIQZWGSSA-N
SMILES
COC1=CC=C(OC)C(C=N/NC(=O)CNC2=CC=C(C)C=C2)=C1
Specifications
Specification SheetAssay (Aqueous acid-base Titration)
≥95.0%
Appearance (Color)
White to cream to brown to gray
Proton NMR
Conforms to structure
Form
Powder
Assay (HPLC)
≥95.0%
Description
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
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