(4-(Prop-1-en-2-yl)phenyl)boronic acid CAS 6962-76-1

Purity 97%+In StockPharmaceutical Standards
CAS No.6962-76-1
Molecular FormulaC16H20N2O
Molecular Weight256.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-(Prop-1-en-2-yl)phenyl)boronic acid CAS 6962-76-1 chemical structure

Description

The occurrence of (4-(Prop-1-en-2-yl)phenyl)boronic acid is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(4-(Prop-1-en-2-yl)phenyl)boronic acid (CAS 6962-76-1), molecular formula C16H20N2O and molecular weight 256.34 g/mol, is a CATO reference standard with documented purity and traceability.

(4-(Prop-1-en-2-yl)phenyl)boronic acid (C16H20N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), (4-(Prop-1-en-2-yl)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 FormulaC16H20N2O
Molecular Weight256.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms2

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