ethyl 1,3-benzothiazole-6-carboxylate CAS 19989-64-1

Purity 97%+In StockPharmaceutical Standards
CAS No.19989-64-1
Molecular FormulaC10H17NO2S
Molecular Weight215.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

ethyl 1,3-benzothiazole-6-carboxylate CAS 19989-64-1 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies ethyl 1,3-benzothiazole-6-carboxylate (CAS 19989-64-1), a certified reference material (molecular formula C10H17NO2S, MW 215.31 g/mol) for analytical method development and quality control.

The molecular framework of ethyl 1,3-benzothiazole-6-carboxylate (C10H17NO2S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

As a certified reference material (CRM), ethyl 1,3-benzothiazole-6-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H17NO2S
Molecular Weight215.31 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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1962
Nitrogen Atoms1
Sulfur Atoms1

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