5-(3-Nitrophenyl)-1-(3-(trifluoromethyl)phenyl)-1h-imidazole-2-thiol CAS 1105189-24-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1105189-24-9
Molecular FormulaC16H10F3N3O2S
Molecular Weight365.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3-Nitrophenyl)-1-(3-(trifluoromethyl)phenyl)-1h-imidazole-2-thiol CAS 1105189-24-9 chemical structure

Description

5-(3-Nitrophenyl)-1-(3-(trifluoromethyl)phenyl)-1h-imidazole-2-thiol (CAS 1105189-24-9), molecular formula C16H10F3N3O2S and molecular weight 365.33 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H10F3N3O2S, 5-(3-Nitrophenyl)-1-(3-(trifluoromethyl)phenyl)-1h-imidazole-2-thiol contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 365.33 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

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 5-(3-Nitrophenyl)-1-(3-(trifluoromethyl)phenyl)-1h-imidazole-2-thiol 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 FormulaC16H10F3N3O2S
Molecular Weight365.33 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

Related Nitrophenyl Standards

Recommended Standards

Why CATO?