2-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)-N-methylethan-1-amine CAS 1142210-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1142210-85-2
Molecular FormulaC11H12FN3O
Molecular Weight221.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)-N-methylethan-1-amine CAS 1142210-85-2 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 2-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)-N-methylethan-1-amine (CAS 1142210-85-2), a certified reference material (molecular formula C11H12FN3O, MW 221.23 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, 2-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)-N-methylethan-1-amine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 221.23 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 2-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)-N-methylethan-1-amine 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 FormulaC11H12FN3O
Molecular Weight221.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3

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