2-Formyl-3-(trifluoromethoxy)phenyboronic acid CAS 1451392-92-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1451392-92-9
Molecular FormulaC8H6BF3O4
Molecular Weight233.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Formyl-3-(trifluoromethoxy)phenyboronic acid CAS 1451392-92-9 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

2-Formyl-3-(trifluoromethoxy)phenyboronic acid (CAS 1451392-92-9) is a high-purity analytical reference standard with the molecular formula C8H6BF3O4 and a molecular weight of 233.94 g/mol.

Based on its molecular formula C8H6BF3O4, 2-Formyl-3-(trifluoromethoxy)phenyboronic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 233.94 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H6BF3O4
Molecular Weight233.94 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing

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