3-Chloro-N-(2-methylnaphthalen-1-yl)benzo[b]thiophene-2-carboxamide CAS 332156-75-9

Purity 97%+In StockPharmaceutical Standards
CAS No.332156-75-9
Molecular FormulaC20H14ClNOS
Molecular Weight351.85 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-N-(2-methylnaphthalen-1-yl)benzo[b]thiophene-2-carboxamide CAS 332156-75-9 chemical structure

Description

Based on its molecular formula C20H14ClNOS, 3-Chloro-N-(2-methylnaphthalen-1-yl)benzo[b]thiophene-2-carboxamide contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 351.85 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.

3-Chloro-N-(2-methylnaphthalen-1-yl)benzo[b]thiophene-2-carboxamide (CAS 332156-75-9), molecular formula C20H14ClNOS and molecular weight 351.85 g/mol, is a CATO reference standard with documented purity and traceability.

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.

CATO manufactures 3-Chloro-N-(2-methylnaphthalen-1-yl)benzo[b]thiophene-2-carboxamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H14ClNOS
Molecular Weight351.85 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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