tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate CAS 1607800-84-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1607800-84-9
Molecular FormulaC15H16BrNO2
Molecular Weight322.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate CAS 1607800-84-9 chemical structure

Description

The molecular framework of tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate (C15H16BrNO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate (CAS 1607800-84-9), a certified reference material (molecular formula C15H16BrNO2, MW 322.20 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 tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate 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 FormulaC15H16BrNO2
Molecular Weight322.20 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentBr-containing
Nitrogen Atoms1

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