Ethyl (3R,4S)-1-benzyl-4-(2-chloro-6-fluorophenyl)pyrrolidine-3-carboxylate CAS 2327184-32-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2327184-32-5
Molecular FormulaC20H21ClFNO2
Molecular Weight361.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl (3R,4S)-1-benzyl-4-(2-chloro-6-fluorophenyl)pyrrolidine-3-carboxylate CAS 2327184-32-5 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.

Ethyl (3R,4S)-1-benzyl-4-(2-chloro-6-fluorophenyl)pyrrolidine-3-carboxylate (CAS 2327184-32-5), molecular formula C20H21ClFNO2 and molecular weight 361.84 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, Ethyl (3R,4S)-1-benzyl-4-(2-chloro-6-fluorophenyl)pyrrolidine-3-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 361.84 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), Ethyl (3R,4S)-1-benzyl-4-(2-chloro-6-fluorophenyl)pyrrolidine-3-carboxylate 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 FormulaC20H21ClFNO2
Molecular Weight361.84 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.)1999
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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