N-((4-((5-Iodopyrimidin-2-yl)oxy)-3-nitrophenyl)carbamoyl)-2-nitrobenzamide CAS 103828-99-5

Purity 97%+In StockPharmaceutical Standards
CAS No.103828-99-5
Molecular FormulaC18H11IN6O7
Molecular Weight550.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((4-((5-Iodopyrimidin-2-yl)oxy)-3-nitrophenyl)carbamoyl)-2-nitrobenzamide CAS 103828-99-5 chemical structure

Description

N-((4-((5-Iodopyrimidin-2-yl)oxy)-3-nitrophenyl)carbamoyl)-2-nitrobenzamide (C18H11IN6O7) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies N-((4-((5-Iodopyrimidin-2-yl)oxy)-3-nitrophenyl)carbamoyl)-2-nitrobenzamide (CAS 103828-99-5), a certified reference material (molecular formula C18H11IN6O7, MW 550.22 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.

As a certified reference material (CRM), N-((4-((5-Iodopyrimidin-2-yl)oxy)-3-nitrophenyl)carbamoyl)-2-nitrobenzamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC18H11IN6O7
Molecular Weight550.22 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore in a cool place (≤25°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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentI-containing
Nitrogen Atoms6

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