1-[3-(Bromomethyl)phenyl]-1H-pyrrole CAS 112596-36-8

Purity 97%+In StockPharmaceutical Standards
CAS No.112596-36-8
Molecular FormulaC11H10BrN
Molecular Weight236.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[3-(Bromomethyl)phenyl]-1H-pyrrole CAS 112596-36-8 chemical structure

Description

The occurrence of 1-[3-(Bromomethyl)phenyl]-1H-pyrrole is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-[3-(Bromomethyl)phenyl]-1H-pyrrole (CAS 112596-36-8), a certified reference material (molecular formula C11H10BrN, MW 236.11 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H10BrN, 1-[3-(Bromomethyl)phenyl]-1H-pyrrole contains a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 236.11 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.

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 FormulaC11H10BrN
Molecular Weight236.11 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
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 ContentBr-containing
Nitrogen Atoms1

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