N-(2-Fluorobenzyl)-2,5-dimethoxyaniline CAS 1021124-41-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1021124-41-3
Molecular FormulaC15H16FNO2
Molecular Weight261.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-Fluorobenzyl)-2,5-dimethoxyaniline CAS 1021124-41-3 chemical structure

Description

N-(2-Fluorobenzyl)-2,5-dimethoxyaniline (CAS 1021124-41-3), molecular formula C15H16FNO2 and molecular weight 261.29 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, N-(2-Fluorobenzyl)-2,5-dimethoxyaniline (C15H16FNO2) 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 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 261.29 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.

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

As a certified reference material (CRM), N-(2-Fluorobenzyl)-2,5-dimethoxyaniline meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC15H16FNO2
Molecular Weight261.29 g/mol
AppearancePale yellow to 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms1

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