3-[(2-Fluorophenyl)methyl]-4,4-dimethyl-1,3-oxazolidine CAS 866157-36-0

Purity 97%+In StockPharmaceutical Standards
CAS No.866157-36-0
Molecular FormulaC12H16FNO
Molecular Weight209.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(2-Fluorophenyl)methyl]-4,4-dimethyl-1,3-oxazolidine CAS 866157-36-0 chemical structure

Description

CATO manufactures 3-[(2-Fluorophenyl)methyl]-4,4-dimethyl-1,3-oxazolidine 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.

3-[(2-Fluorophenyl)methyl]-4,4-dimethyl-1,3-oxazolidine (CAS 866157-36-0) is a high-purity analytical reference standard with the molecular formula C12H16FNO and a molecular weight of 209.26 g/mol.

The molecular framework of 3-[(2-Fluorophenyl)methyl]-4,4-dimethyl-1,3-oxazolidine (C12H16FNO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC12H16FNO
Molecular Weight209.26 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
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1

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