Methyl 4-chloro-3-methylthieno[3,2-c]pyridine-7-carboxylate CAS 1360901-67-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1360901-67-2
Molecular FormulaC10H8ClNO2S
Molecular Weight241.69 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-chloro-3-methylthieno[3,2-c]pyridine-7-carboxylate CAS 1360901-67-2 chemical structure

Description

CATO manufactures Methyl 4-chloro-3-methylthieno[3,2-c]pyridine-7-carboxylate 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.

CATO supplies Methyl 4-chloro-3-methylthieno[3,2-c]pyridine-7-carboxylate (CAS 1360901-67-2), a certified reference material (molecular formula C10H8ClNO2S, MW 241.69 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, Methyl 4-chloro-3-methylthieno[3,2-c]pyridine-7-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 241.69 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC10H8ClNO2S
Molecular Weight241.69 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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