Methyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate CAS 847755-88-8

Purity 97%+In StockPharmaceutical Standards
CAS No.847755-88-8
Molecular FormulaC7H6F3NO2S
Molecular Weight225.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate CAS 847755-88-8 chemical structure

Description

CATO supplies Methyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate (CAS 847755-88-8), a certified reference material (molecular formula C7H6F3NO2S, MW 225.19 g/mol) for analytical method development and quality control.

Based on its molecular formula C7H6F3NO2S, Methyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 225.19 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.

As a certified reference material (CRM), Methyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate 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 FormulaC7H6F3NO2S
Molecular Weight225.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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