Methyl 3-(4-((3-fluorophenyl)sulfonamido)phenoxy)thiophene-2-carboxylate CAS 900015-22-7

Purity 97%+In StockPharmaceutical Standards
CAS No.900015-22-7
Molecular FormulaC18H14FNO5S2
Molecular Weight407.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(4-((3-fluorophenyl)sulfonamido)phenoxy)thiophene-2-carboxylate CAS 900015-22-7 chemical structure

Description

Methyl 3-(4-((3-fluorophenyl)sulfonamido)phenoxy)thiophene-2-carboxylate (CAS 900015-22-7) is a high-purity analytical reference standard with the molecular formula C18H14FNO5S2 and a molecular weight of 407.44 g/mol.

Based on its molecular formula C18H14FNO5S2, Methyl 3-(4-((3-fluorophenyl)sulfonamido)phenoxy)thiophene-2-carboxylate contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 407.44 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC18H14FNO5S2
Molecular Weight407.44 g/mol
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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