6-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonyl chloride CAS 1160248-88-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1160248-88-3
Molecular FormulaC10H11ClOS
Molecular Weight214.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonyl chloride CAS 1160248-88-3 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.

CATO supplies 6-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonyl chloride (CAS 1160248-88-3), a certified reference material (molecular formula C10H11ClOS, MW 214.71 g/mol) for analytical method development and quality control.

Based on its molecular formula C10H11ClOS, 6-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonyl chloride contains sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 214.71 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.

CATO manufactures 6-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonyl chloride 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 FormulaC10H11ClOS
Molecular Weight214.71 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Sulfur Atoms1

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