4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)thiophen-3-yl)-1,3,2-dioxaborolane CAS 2246611-07-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2246611-07-2
Molecular FormulaC11H14BF3O2S
Molecular Weight278.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)thiophen-3-yl)-1,3,2-dioxaborolane CAS 2246611-07-2 chemical structure

Description

As a certified reference material (CRM), 4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)thiophen-3-yl)-1,3,2-dioxaborolane 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.

4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)thiophen-3-yl)-1,3,2-dioxaborolane (CAS 2246611-07-2), molecular formula C11H14BF3O2S and molecular weight 278.10 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, 4,4,5,5-Tetramethyl-2-(2-(trifluoromethyl)thiophen-3-yl)-1,3,2-dioxaborolane is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 278.10 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

Physical & Chemical Properties

Molecular FormulaC11H14BF3O2S
Molecular Weight278.10 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.5
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1998
Halogen ContentF-containing
Sulfur Atoms1

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