Ethyl 4-(bromomethyl)-1,2,3-thiadiazole-5-carboxylate CAS 59944-59-1

Purity 97%+In StockPharmaceutical Standards
CAS No.59944-59-1
Molecular FormulaC6H7BrN2O2S
Molecular Weight251.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 4-(bromomethyl)-1,2,3-thiadiazole-5-carboxylate CAS 59944-59-1 chemical structure

Description

Ethyl 4-(bromomethyl)-1,2,3-thiadiazole-5-carboxylate (CAS 59944-59-1), molecular formula C6H7BrN2O2S and molecular weight 251.10 g/mol, is a CATO reference standard with documented purity and traceability.

Ethyl 4-(bromomethyl)-1,2,3-thiadiazole-5-carboxylate (C6H7BrN2O2S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

CATO manufactures Ethyl 4-(bromomethyl)-1,2,3-thiadiazole-5-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.

Physical & Chemical Properties

Molecular FormulaC6H7BrN2O2S
Molecular Weight251.10 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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