4-Bromoisoquinoline-5-sulfonyl chloride hydrochloride CAS 1203176-80-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1203176-80-0
Molecular FormulaC9H5BrClNO2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Bromoisoquinoline-5-sulfonyl chloride hydrochloride CAS 1203176-80-0 chemical structure

Description

Based on its molecular formula C9H5BrClNO2SHCl, 4-Bromoisoquinoline-5-sulfonyl chloride hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 343.02 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.

CATO supplies 4-Bromoisoquinoline-5-sulfonyl chloride hydrochloride (CAS 1203176-80-0), a certified reference material (molecular formula C9H5BrClNO2SHCl, MW 343.02 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.

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 FormulaC9H5BrClNO2S HCl
Molecular Weight343.02 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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