N-(2,5-Dimethylphenyl)-4-morpholinoquinazolin-2-amine hydrochloride CAS 1078730-84-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1078730-84-3
Molecular FormulaC20H22N4O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2,5-Dimethylphenyl)-4-morpholinoquinazolin-2-amine hydrochloride CAS 1078730-84-3 chemical structure

Description

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

CATO supplies N-(2,5-Dimethylphenyl)-4-morpholinoquinazolin-2-amine hydrochloride (CAS 1078730-84-3), a certified reference material (molecular formula C20H22N4OHCl, MW 370.88 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, N-(2,5-Dimethylphenyl)-4-morpholinoquinazolin-2-amine hydrochloride is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 370.88 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 manufactures N-(2,5-Dimethylphenyl)-4-morpholinoquinazolin-2-amine hydrochloride 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 FormulaC20H22N4O HCl
Molecular Weight370.88 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 DMSO, DMF, methanol
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.)1988
Halogen ContentCl-containing
Nitrogen Atoms4

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