tert-butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate CAS 951259-22-6

Purity 97%+In StockPharmaceutical Standards
CAS No.951259-22-6
Molecular FormulaC14H20BrNO2S
Molecular Weight346.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate CAS 951259-22-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including tert-butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate.

CATO supplies tert-butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate (CAS 951259-22-6), a certified reference material (molecular formula C14H20BrNO2S, MW 346.28 g/mol) for analytical method development and quality control.

The molecular framework of tert-butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate (C14H20BrNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC14H20BrNO2S
Molecular Weight346.28 g/mol
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.)1987
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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