tert-Butyl ((1-(2-chloronicotinoyl)piperidin-3-yl)methyl)carbamate CAS 1353974-41-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1353974-41-0
Molecular FormulaC17H24ClN3O3
Molecular Weight353.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl ((1-(2-chloronicotinoyl)piperidin-3-yl)methyl)carbamate CAS 1353974-41-0 chemical structure

Description

As a certified reference material (CRM), tert-Butyl ((1-(2-chloronicotinoyl)piperidin-3-yl)methyl)carbamate 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.

CATO supplies tert-Butyl ((1-(2-chloronicotinoyl)piperidin-3-yl)methyl)carbamate (CAS 1353974-41-0), a certified reference material (molecular formula C17H24ClN3O3, MW 353.84 g/mol) for analytical method development and quality control.

Based on its molecular formula C17H24ClN3O3, tert-Butyl ((1-(2-chloronicotinoyl)piperidin-3-yl)methyl)carbamate contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 353.84 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC17H24ClN3O3
Molecular Weight353.84 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; 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.)1991
Halogen ContentCl-containing
Nitrogen Atoms3

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