5-(2-Aminothiazol-4-yl)-2-hydroxybenzyl acetate CAS 890096-19-2

Purity 97%+In StockPharmaceutical Standards
CAS No.890096-19-2
Molecular FormulaC12H12N2O3S
Molecular Weight264.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-Aminothiazol-4-yl)-2-hydroxybenzyl acetate CAS 890096-19-2 chemical structure

Description

CATO manufactures 5-(2-Aminothiazol-4-yl)-2-hydroxybenzyl acetate 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 5-(2-Aminothiazol-4-yl)-2-hydroxybenzyl acetate (CAS 890096-19-2), a certified reference material (molecular formula C12H12N2O3S, MW 264.30 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H12N2O3S, 5-(2-Aminothiazol-4-yl)-2-hydroxybenzyl acetate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 264.30 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC12H12N2O3S
Molecular Weight264.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2
Sulfur Atoms1

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