4-amino-N-(5-bromo-2-hydroxyphenyl)-3-methylbenzamide CAS 1522495-64-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1522495-64-2
Molecular FormulaC14H13BrN2O2
Molecular Weight321.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-amino-N-(5-bromo-2-hydroxyphenyl)-3-methylbenzamide CAS 1522495-64-2 chemical structure

Description

Based on its molecular formula C14H13BrN2O2, 4-amino-N-(5-bromo-2-hydroxyphenyl)-3-methylbenzamide 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 321.17 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 4-amino-N-(5-bromo-2-hydroxyphenyl)-3-methylbenzamide (CAS 1522495-64-2), a certified reference material (molecular formula C14H13BrN2O2, MW 321.17 g/mol) for analytical method development and quality control.

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

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 FormulaC14H13BrN2O2
Molecular Weight321.17 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentBr-containing
Nitrogen Atoms2

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