2-(chloromethyl)-5-(5-ethyl-4-methylthien-2-yl)-1,3,4-oxadiazole CAS 796106-51-9

Purity 97%+In StockPharmaceutical Standards
CAS No.796106-51-9
Molecular FormulaC10H11ClN2OS
Molecular Weight242.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(chloromethyl)-5-(5-ethyl-4-methylthien-2-yl)-1,3,4-oxadiazole CAS 796106-51-9 chemical structure

Description

2-(chloromethyl)-5-(5-ethyl-4-methylthien-2-yl)-1,3,4-oxadiazole (CAS 796106-51-9) is a high-purity analytical reference standard with the molecular formula C10H11ClN2OS and a molecular weight of 242.73 g/mol.

Based on its molecular formula C10H11ClN2OS, 2-(chloromethyl)-5-(5-ethyl-4-methylthien-2-yl)-1,3,4-oxadiazole contains a nitrogen-containing heterocyclic scaffold, 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 242.73 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 2-(chloromethyl)-5-(5-ethyl-4-methylthien-2-yl)-1,3,4-oxadiazole 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 FormulaC10H11ClN2OS
Molecular Weight242.73 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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