(3S)-Methyl 2-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate hydrochloride CAS 1049755-89-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1049755-89-6
Molecular FormulaC12H13Cl2NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S)-Methyl 2-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate hydrochloride CAS 1049755-89-6 chemical structure

Description

The molecular framework of (3S)-Methyl 2-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate hydrochloride (C12H13Cl2NO2HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

(3S)-Methyl 2-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate hydrochloride (CAS 1049755-89-6) is a high-purity analytical reference standard with the molecular formula C12H13Cl2NO2HCl and a molecular weight of 310.60 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.

CATO manufactures (3S)-Methyl 2-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate hydrochloride 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.

Physical & Chemical Properties

Molecular FormulaC12H13Cl2NO2 HCl
Molecular Weight310.60 g/mol
AppearanceOff-white to pale 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms1

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