4-(Trifluoromethylthio)benzyl alcohol 4-trifluoromethylthiobenzyl alcohol 4-trifluomethylthio benzyl alcohol (4-trifluoromethylsulfanyl-phenyl)-methanol 4-trifluoromethylthiobenzylalcohol 4-(trifluoromethylthio)benzylalcohol (4-[(trifluoromethyl)sulfanyl]phenyl)methanol 4-(Trifluoromethylthio)benzoic acid 4-Trifluoromethylsulfanylbenzoic acid 56456-52-1 CAS 56456-52-1

Purity 97%+In StockPharmaceutical Standards
CAS No.56456-52-1
Molecular FormulaC8H7F3OS
Molecular Weight208.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Trifluoromethylthio)benzyl alcohol 4-trifluoromethylthiobenzyl alcohol 4-trifluomethylthio benzyl alcohol (4-trifluoromethylsulfanyl-phenyl)-methanol 4-trifluoromethylthiobenzylalcohol 4-(trifluoromethylthio)benzylalcohol (4-[(trifluoromethyl)sulfanyl]phenyl)methanol 4-(Trifluoromethylthio)benzoic acid 4-Trifluoromethylsulfanylbenzoic acid 56456-52-1 CAS 56456-52-1 chemical structure

Description

The molecular framework of 4-(Trifluoromethylthio)benzyl alcohol 4-trifluoromethylthiobenzyl alcohol 4-trifluomethylthio benzyl alcohol (4-trifluoromethylsulfanyl-phenyl)-methanol 4-trifluoromethylthiobenzylalcohol 4-(trifluoromethylthio)benzylalcohol (4-[(trifluoromethyl)sulfanyl]phenyl)methanol 4-(Trifluoromethylthio)benzoic acid 4-Trifluoromethylsulfanylbenzoic acid 56456-52-1 (C8H7F3OS) is characterized by sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

4-(Trifluoromethylthio)benzyl alcohol 4-trifluoromethylthiobenzyl alcohol 4-trifluomethylthio benzyl alcohol (4-trifluoromethylsulfanyl-phenyl)-methanol 4-trifluoromethylthiobenzylalcohol 4-(trifluoromethylthio)benzylalcohol (4-[(trifluoromethyl)sulfanyl]phenyl)methanol 4-(Trifluoromethylthio)benzoic acid 4-Trifluoromethylsulfanylbenzoic acid 56456-52-1 (CAS 56456-52-1), molecular formula C8H7F3OS and molecular weight 208.20 g/mol, is a CATO reference standard with documented purity and traceability.

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

CATO manufactures 4-(Trifluoromethylthio)benzyl alcohol 4-trifluoromethylthiobenzyl alcohol 4-trifluomethylthio benzyl alcohol (4-trifluoromethylsulfanyl-phenyl)-methanol 4-trifluoromethylthiobenzylalcohol 4-(trifluoromethylthio)benzylalcohol (4-[(trifluoromethyl)sulfanyl]phenyl)methanol 4-(Trifluoromethylthio)benzoic acid 4-Trifluoromethylsulfanylbenzoic acid 56456-52-1 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H7F3OS
Molecular Weight208.20 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Halogen ContentF-containing
Sulfur Atoms1

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