Pentafluorophenyl-4-methyl-1,3-thiazole-2-sulfonate CAS 1421602-12-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1421602-12-1
Molecular FormulaC10H4F5NO3S2
Molecular Weight345.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Pentafluorophenyl-4-methyl-1,3-thiazole-2-sulfonate CAS 1421602-12-1 chemical structure

Description

As a certified reference material (CRM), Pentafluorophenyl-4-methyl-1,3-thiazole-2-sulfonate 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.

Pentafluorophenyl-4-methyl-1,3-thiazole-2-sulfonate (CAS 1421602-12-1), molecular formula C10H4F5NO3S2 and molecular weight 345.27 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, Pentafluorophenyl-4-methyl-1,3-thiazole-2-sulfonate (C10H4F5NO3S2) 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 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 345.27 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC10H4F5NO3S2
Molecular Weight345.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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