2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid CAS 1087792-10-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1087792-10-6
Molecular FormulaC12H10FNO2S
Molecular Weight251.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid CAS 1087792-10-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 251.28 g/mol gives 2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid (CAS 1087792-10-6) is a high-purity analytical reference standard with the molecular formula C12H10FNO2S and a molecular weight of 251.28 g/mol.

The molecular framework of 2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid (C12H10FNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

CATO manufactures 2-(4-fluorobenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid 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 FormulaC12H10FNO2S
Molecular Weight251.28 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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