4-Chloro-3-fluoro-2-morpholinomethyl benzophenone CAS 898750-65-7

Purity 97%+In StockPharmaceutical Standards
CAS No.898750-65-7
Molecular FormulaC18H17ClFNO2
Molecular Weight333.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-3-fluoro-2-morpholinomethyl benzophenone CAS 898750-65-7 chemical structure

Description

The molecular framework of 4-Chloro-3-fluoro-2-morpholinomethyl benzophenone (C18H17ClFNO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

4-Chloro-3-fluoro-2-morpholinomethyl benzophenone (CAS 898750-65-7) is a high-purity analytical reference standard with the molecular formula C18H17ClFNO2 and a molecular weight of 333.78 g/mol.

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), 4-Chloro-3-fluoro-2-morpholinomethyl benzophenone 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 FormulaC18H17ClFNO2
Molecular Weight333.78 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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