Methyl (E)-2-(((methoxyamino)methylene)amino)thiophene-3-carboxylate CAS 338750-41-7

Purity 97%+In StockPharmaceutical Standards
CAS No.338750-41-7
Molecular FormulaC8H10N2O3S
Molecular Weight214.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (E)-2-(((methoxyamino)methylene)amino)thiophene-3-carboxylate CAS 338750-41-7 chemical structure

Description

Methyl (E)-2-(((methoxyamino)methylene)amino)thiophene-3-carboxylate (CAS 338750-41-7) is a high-purity analytical reference standard with the molecular formula C8H10N2O3S and a molecular weight of 214.24 g/mol.

Based on its molecular formula C8H10N2O3S, Methyl (E)-2-(((methoxyamino)methylene)amino)thiophene-3-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 214.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

As a certified reference material (CRM), Methyl (E)-2-(((methoxyamino)methylene)amino)thiophene-3-carboxylate 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.

Physical & Chemical Properties

Molecular FormulaC8H10N2O3S
Molecular Weight214.24 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
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2
Sulfur Atoms1

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