3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]propanoic acid CAS 885527-39-9

Purity 97%+In StockPharmaceutical Standards
CAS No.885527-39-9
Molecular FormulaC11H8F3NO2S
Molecular Weight275.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]propanoic acid CAS 885527-39-9 chemical structure

Description

CATO manufactures 3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]propanoic acid 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.

3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]propanoic acid (CAS 885527-39-9) is a high-purity analytical reference standard with the molecular formula C11H8F3NO2S and a molecular weight of 275.25 g/mol.

3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]propanoic acid (C11H8F3NO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC11H8F3NO2S
Molecular Weight275.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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