Methyl 4-phenyl-3-(1H-pyrrol-1-yl)thiophene-2-carboxylate CAS 156274-05-4

Purity 97%+In StockPharmaceutical Standards
CAS No.156274-05-4
Molecular FormulaC16H13NO2S
Molecular Weight283.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-phenyl-3-(1H-pyrrol-1-yl)thiophene-2-carboxylate CAS 156274-05-4 chemical structure

Description

The occurrence of Methyl 4-phenyl-3-(1H-pyrrol-1-yl)thiophene-2-carboxylate is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Methyl 4-phenyl-3-(1H-pyrrol-1-yl)thiophene-2-carboxylate (CAS 156274-05-4), molecular formula C16H13NO2S and molecular weight 283.34 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, Methyl 4-phenyl-3-(1H-pyrrol-1-yl)thiophene-2-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 283.34 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).

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 FormulaC16H13NO2S
Molecular Weight283.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2001
Nitrogen Atoms1
Sulfur Atoms1

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