2-((3-Fluoro-4-methylphenyl)amino)-2-oxoethyl 5-methylthiophene-2-carboxylate CAS 848372-89-4

Purity 97%+In StockPharmaceutical Standards
CAS No.848372-89-4
Molecular FormulaC15H14FNO3S
Molecular Weight307.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((3-Fluoro-4-methylphenyl)amino)-2-oxoethyl 5-methylthiophene-2-carboxylate CAS 848372-89-4 chemical structure

Description

Structurally, 2-((3-Fluoro-4-methylphenyl)amino)-2-oxoethyl 5-methylthiophene-2-carboxylate (C15H14FNO3S) 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 307.34 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.

CATO supplies 2-((3-Fluoro-4-methylphenyl)amino)-2-oxoethyl 5-methylthiophene-2-carboxylate (CAS 848372-89-4), a certified reference material (molecular formula C15H14FNO3S, MW 307.34 g/mol) for analytical method development and quality control.

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

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 FormulaC15H14FNO3S
Molecular Weight307.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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