2-(3-(1,1,2,2-Tetrafluoroethoxy)phenyl)ethanethiol CAS 1443347-73-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1443347-73-6
Molecular FormulaC10H10F4OS
Molecular Weight254.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-(1,1,2,2-Tetrafluoroethoxy)phenyl)ethanethiol CAS 1443347-73-6 chemical structure

Description

Structurally, 2-(3-(1,1,2,2-Tetrafluoroethoxy)phenyl)ethanethiol (C10H10F4OS) contains sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 254.24 g/mol, it falls into the medium-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

2-(3-(1,1,2,2-Tetrafluoroethoxy)phenyl)ethanethiol (CAS 1443347-73-6) is a high-purity analytical reference standard with the molecular formula C10H10F4OS and a molecular weight of 254.24 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), 2-(3-(1,1,2,2-Tetrafluoroethoxy)phenyl)ethanethiol 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 FormulaC10H10F4OS
Molecular Weight254.24 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
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Sulfur Atoms1

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