2-(5-Bromothiophen-2-yl)-4-chloro-6-methylpyrimidine CAS 1155155-56-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1155155-56-8
Molecular FormulaC9H6BrClN2S
Molecular Weight289.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(5-Bromothiophen-2-yl)-4-chloro-6-methylpyrimidine CAS 1155155-56-8 chemical structure

Description

The molecular framework of 2-(5-Bromothiophen-2-yl)-4-chloro-6-methylpyrimidine (C9H6BrClN2S) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine/bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 2-(5-Bromothiophen-2-yl)-4-chloro-6-methylpyrimidine (CAS 1155155-56-8), a certified reference material (molecular formula C9H6BrClN2S, MW 289.58 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 2-(5-Bromothiophen-2-yl)-4-chloro-6-methylpyrimidine 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 FormulaC9H6BrClN2S
Molecular Weight289.58 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl/Br-containing
Nitrogen Atoms2
Sulfur Atoms1

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