3-Cyclopropoxy-6-fluoro-N-methylcyclohexa-2,4-diene-1-carboxamide CAS 1243390-89-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1243390-89-7
Molecular FormulaC11H14FNO2
Molecular Weight211.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Cyclopropoxy-6-fluoro-N-methylcyclohexa-2,4-diene-1-carboxamide CAS 1243390-89-7 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 3-Cyclopropoxy-6-fluoro-N-methylcyclohexa-2,4-diene-1-carboxamide (CAS 1243390-89-7), a certified reference material (molecular formula C11H14FNO2, MW 211.23 g/mol) for analytical method development and quality control.

Structurally, 3-Cyclopropoxy-6-fluoro-N-methylcyclohexa-2,4-diene-1-carboxamide (C11H14FNO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 211.23 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H14FNO2
Molecular Weight211.23 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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