5-(3,4-Dihydro-2H-pyrrol-5-yl)-2-isopropoxypyridine CAS 1352487-45-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1352487-45-6
Molecular FormulaC12H16N2O
Molecular Weight204.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3,4-Dihydro-2H-pyrrol-5-yl)-2-isopropoxypyridine CAS 1352487-45-6 chemical structure

Description

The occurrence of 5-(3,4-Dihydro-2H-pyrrol-5-yl)-2-isopropoxypyridine is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 5-(3,4-Dihydro-2H-pyrrol-5-yl)-2-isopropoxypyridine (CAS 1352487-45-6), a certified reference material (molecular formula C12H16N2O, MW 204.27 g/mol) for analytical method development and quality control.

5-(3,4-Dihydro-2H-pyrrol-5-yl)-2-isopropoxypyridine (C12H16N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; 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.

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.

Physical & Chemical Properties

Molecular FormulaC12H16N2O
Molecular Weight204.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms2

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