Methyl 7-amino-2-(4-methoxyphenyl)-3-oxo-2H,3H-thieno[3,2-c]pyridazine-6-carboxylate CAS 338395-94-1

Purity 97%+In StockPharmaceutical Standards
CAS No.338395-94-1
Molecular FormulaC15H13N3O4S
Molecular Weight331.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 7-amino-2-(4-methoxyphenyl)-3-oxo-2H,3H-thieno[3,2-c]pyridazine-6-carboxylate CAS 338395-94-1 chemical structure

Description

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.

Methyl 7-amino-2-(4-methoxyphenyl)-3-oxo-2H,3H-thieno[3,2-c]pyridazine-6-carboxylate (CAS 338395-94-1) is a high-purity analytical reference standard with the molecular formula C15H13N3O4S and a molecular weight of 331.35 g/mol.

The molecular framework of Methyl 7-amino-2-(4-methoxyphenyl)-3-oxo-2H,3H-thieno[3,2-c]pyridazine-6-carboxylate (C15H13N3O4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC15H13N3O4S
Molecular Weight331.35 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3
Sulfur Atoms1

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