4-(4-Bromophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid CAS 78860-79-4

Purity 97%+In StockPharmaceutical Standards
CAS No.78860-79-4
Molecular FormulaC18H14BrNO3
Molecular Weight372.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Bromophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid CAS 78860-79-4 chemical structure

Description

CATO manufactures 4-(4-Bromophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid 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.

4-(4-Bromophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid (CAS 78860-79-4), molecular formula C18H14BrNO3 and molecular weight 372.21 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-(4-Bromophenyl)-2-(1H-indol-3-yl)-4-oxobutanoic acid (C18H14BrNO3) is characterized by a steroid core, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC18H14BrNO3
Molecular Weight372.21 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1979
Halogen ContentBr-containing
Nitrogen Atoms1

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