N-(3-Iodophenyl)-6-nitroquinazolin-4-amine CAS 733009-36-4

Purity 97%+In StockPharmaceutical Standards
CAS No.733009-36-4
Molecular FormulaC14H9IN4O2
Molecular Weight392.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Iodophenyl)-6-nitroquinazolin-4-amine CAS 733009-36-4 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(3-Iodophenyl)-6-nitroquinazolin-4-amine.

N-(3-Iodophenyl)-6-nitroquinazolin-4-amine (CAS 733009-36-4) is a high-purity analytical reference standard with the molecular formula C14H9IN4O2 and a molecular weight of 392.15 g/mol.

The molecular framework of N-(3-Iodophenyl)-6-nitroquinazolin-4-amine (C14H9IN4O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures N-(3-Iodophenyl)-6-nitroquinazolin-4-amine 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 FormulaC14H9IN4O2
Molecular Weight392.15 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentI-containing
Nitrogen Atoms4

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