3-(2-Nitro-4-(trifluoromethyl)phenoxy)thiophene-2-carboxylic acid CAS 252026-58-7

Purity 97%+In StockPharmaceutical Standards
CAS No.252026-58-7
Molecular FormulaC12H6F3NO5S
Molecular Weight333.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Nitro-4-(trifluoromethyl)phenoxy)thiophene-2-carboxylic acid CAS 252026-58-7 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 3-(2-Nitro-4-(trifluoromethyl)phenoxy)thiophene-2-carboxylic acid (CAS 252026-58-7), a certified reference material (molecular formula C12H6F3NO5S, MW 333.24 g/mol) for analytical method development and quality control.

Structurally, 3-(2-Nitro-4-(trifluoromethyl)phenoxy)thiophene-2-carboxylic acid (C12H6F3NO5S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 333.24 g/mol, it falls into the moderately-high-molecular-weight range. 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).

As a certified reference material (CRM), 3-(2-Nitro-4-(trifluoromethyl)phenoxy)thiophene-2-carboxylic acid 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 FormulaC12H6F3NO5S
Molecular Weight333.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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