tert-Butyl 2-Chloro-5-fluoroquinazoline-4-acetate CAS 1312784-45-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1312784-45-4
Molecular FormulaC14H14ClFN2O2
Molecular Weight296.72 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 2-Chloro-5-fluoroquinazoline-4-acetate CAS 1312784-45-4 chemical structure

Description

Based on its molecular formula C14H14ClFN2O2, tert-Butyl 2-Chloro-5-fluoroquinazoline-4-acetate contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 296.72 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

tert-Butyl 2-Chloro-5-fluoroquinazoline-4-acetate (CAS 1312784-45-4) is a high-purity analytical reference standard with the molecular formula C14H14ClFN2O2 and a molecular weight of 296.72 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), tert-Butyl 2-Chloro-5-fluoroquinazoline-4-acetate 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 FormulaC14H14ClFN2O2
Molecular Weight296.72 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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