4-(4-Chlorophenyl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazol-2-amine CAS 914660-36-9

Purity 97%+In StockPharmaceutical Standards
CAS No.914660-36-9
Molecular FormulaC16H10ClF3N2OS
Molecular Weight370.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Chlorophenyl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazol-2-amine CAS 914660-36-9 chemical structure

Description

4-(4-Chlorophenyl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazol-2-amine (C16H10ClF3N2OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

4-(4-Chlorophenyl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazol-2-amine (CAS 914660-36-9) is a high-purity analytical reference standard with the molecular formula C16H10ClF3N2OS and a molecular weight of 370.78 g/mol.

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-(4-Chlorophenyl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazol-2-amine 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 FormulaC16H10ClF3N2OS
Molecular Weight370.78 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Nitrogen Atoms2
Sulfur Atoms1

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