(5-Bromothiophen-3-yl)(4-(hydroxymethyl)piperidin-1-yl)methanone CAS 1154926-17-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1154926-17-6
Molecular FormulaC11H14BrNO2S
Molecular Weight304.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-Bromothiophen-3-yl)(4-(hydroxymethyl)piperidin-1-yl)methanone CAS 1154926-17-6 chemical structure

Description

Structurally, (5-Bromothiophen-3-yl)(4-(hydroxymethyl)piperidin-1-yl)methanone (C11H14BrNO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 304.20 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies (5-Bromothiophen-3-yl)(4-(hydroxymethyl)piperidin-1-yl)methanone (CAS 1154926-17-6), a certified reference material (molecular formula C11H14BrNO2S, MW 304.20 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures (5-Bromothiophen-3-yl)(4-(hydroxymethyl)piperidin-1-yl)methanone 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 FormulaC11H14BrNO2S
Molecular Weight304.20 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.)1989
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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