(3-Fluoro-4-((4-fluorophenyl)sulfonamido)phenyl)boronic acid CAS 1314069-46-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1314069-46-9
Molecular FormulaC12H10BF2NO4S
Molecular Weight313.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Fluoro-4-((4-fluorophenyl)sulfonamido)phenyl)boronic acid CAS 1314069-46-9 chemical structure

Description

The molecular framework of (3-Fluoro-4-((4-fluorophenyl)sulfonamido)phenyl)boronic acid (C12H10BF2NO4S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

(3-Fluoro-4-((4-fluorophenyl)sulfonamido)phenyl)boronic acid (CAS 1314069-46-9) is a high-purity analytical reference standard with the molecular formula C12H10BF2NO4S and a molecular weight of 313.08 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), (3-Fluoro-4-((4-fluorophenyl)sulfonamido)phenyl)boronic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H10BF2NO4S
Molecular Weight313.08 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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