[4-(Trifluoromethyl)phenyl]methyl N-(4-methyl-1,2,3-thiadiazol-5-yl)carbamate CAS 338960-84-2

Purity 97%+In StockPharmaceutical Standards
CAS No.338960-84-2
Molecular FormulaC12H10F3N3O2S
Molecular Weight317.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[4-(Trifluoromethyl)phenyl]methyl N-(4-methyl-1,2,3-thiadiazol-5-yl)carbamate CAS 338960-84-2 chemical structure

Description

[4-(Trifluoromethyl)phenyl]methyl N-(4-methyl-1,2,3-thiadiazol-5-yl)carbamate (CAS 338960-84-2), molecular formula C12H10F3N3O2S and molecular weight 317.29 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, [4-(Trifluoromethyl)phenyl]methyl N-(4-methyl-1,2,3-thiadiazol-5-yl)carbamate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 317.29 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC12H10F3N3O2S
Molecular Weight317.29 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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Why CATO?