Methyl 2-(2-chloropropanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate CAS 731012-07-0

Purity 97%+In StockPharmaceutical Standards
CAS No.731012-07-0
Molecular FormulaC13H16ClNO3S
Molecular Weight301.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-(2-chloropropanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate CAS 731012-07-0 chemical structure

Description

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.

Methyl 2-(2-chloropropanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate (CAS 731012-07-0), molecular formula C13H16ClNO3S and molecular weight 301.79 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C13H16ClNO3S, Methyl 2-(2-chloropropanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 301.79 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.

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 FormulaC13H16ClNO3S
Molecular Weight301.79 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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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