N-(3-Chloro-4-fluorobenzyl)-4-ethyl-2-(1H-pyrrol-1-yl)thiazole-5-carboxamide CAS 1243072-49-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1243072-49-2
Molecular FormulaC17H15ClFN3OS
Molecular Weight363.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Chloro-4-fluorobenzyl)-4-ethyl-2-(1H-pyrrol-1-yl)thiazole-5-carboxamide CAS 1243072-49-2 chemical structure

Description

CATO manufactures N-(3-Chloro-4-fluorobenzyl)-4-ethyl-2-(1H-pyrrol-1-yl)thiazole-5-carboxamide 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.

N-(3-Chloro-4-fluorobenzyl)-4-ethyl-2-(1H-pyrrol-1-yl)thiazole-5-carboxamide (CAS 1243072-49-2) is a high-purity analytical reference standard with the molecular formula C17H15ClFN3OS and a molecular weight of 363.84 g/mol.

N-(3-Chloro-4-fluorobenzyl)-4-ethyl-2-(1H-pyrrol-1-yl)thiazole-5-carboxamide (C17H15ClFN3OS) contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC17H15ClFN3OS
Molecular Weight363.84 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms3
Sulfur Atoms1

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