tert-Butyl 6-bromoquinoline-4-carboxylate CAS 2374782-77-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2374782-77-9
Molecular FormulaC14H14BrNO2
Molecular Weight308.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 6-bromoquinoline-4-carboxylate CAS 2374782-77-9 chemical structure

Description

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.

tert-Butyl 6-bromoquinoline-4-carboxylate (CAS 2374782-77-9), molecular formula C14H14BrNO2 and molecular weight 308.17 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C14H14BrNO2, tert-Butyl 6-bromoquinoline-4-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 308.17 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures tert-Butyl 6-bromoquinoline-4-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 FormulaC14H14BrNO2
Molecular Weight308.17 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.)1999
Halogen ContentBr-containing
Nitrogen Atoms1

Recommended Standards

Why CATO?