2-(4-Bromophenyl)-1-methyl-1H-indole-3-carbaldehyde CAS 61843-46-7

Purity 97%+In StockPharmaceutical Standards
CAS No.61843-46-7
Molecular FormulaC16H12BrNO
Molecular Weight314.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromophenyl)-1-methyl-1H-indole-3-carbaldehyde CAS 61843-46-7 chemical structure

Description

Structurally, 2-(4-Bromophenyl)-1-methyl-1H-indole-3-carbaldehyde (C16H12BrNO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 314.18 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2-(4-Bromophenyl)-1-methyl-1H-indole-3-carbaldehyde (CAS 61843-46-7) is a high-purity analytical reference standard with the molecular formula C16H12BrNO and a molecular weight of 314.18 g/mol.

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-(4-Bromophenyl)-1-methyl-1H-indole-3-carbaldehyde 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 FormulaC16H12BrNO
Molecular Weight314.18 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
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentBr-containing
Nitrogen Atoms1

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