(2S,4S)-1-(tert-Butoxycarbonyl)-4-(4-chloro-2-methylphenoxy)-2-pyrrolidinecarboxylic acid CAS 869682-07-5

Purity 97%+In StockPharmaceutical Standards
CAS No.869682-07-5
Molecular FormulaC17H22ClNO5
Molecular Weight355.81 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2S,4S)-1-(tert-Butoxycarbonyl)-4-(4-chloro-2-methylphenoxy)-2-pyrrolidinecarboxylic acid CAS 869682-07-5 chemical structure

Description

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.

CATO supplies (2S,4S)-1-(tert-Butoxycarbonyl)-4-(4-chloro-2-methylphenoxy)-2-pyrrolidinecarboxylic acid (CAS 869682-07-5), a certified reference material (molecular formula C17H22ClNO5, MW 355.81 g/mol) for analytical method development and quality control.

(2S,4S)-1-(tert-Butoxycarbonyl)-4-(4-chloro-2-methylphenoxy)-2-pyrrolidinecarboxylic acid (C17H22ClNO5) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC17H22ClNO5
Molecular Weight355.81 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms1

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