4-Chloro-5,6-dihydrobenzo[h]quinazoline CAS 57711-36-1

Purity 97%+In StockPharmaceutical Standards
CAS No.57711-36-1
Molecular FormulaC12H9ClN2
Molecular Weight216.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-5,6-dihydrobenzo[h]quinazoline CAS 57711-36-1 chemical structure

Description

Based on its molecular formula C12H9ClN2, 4-Chloro-5,6-dihydrobenzo[h]quinazoline contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 216.67 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.

CATO supplies 4-Chloro-5,6-dihydrobenzo[h]quinazoline (CAS 57711-36-1), a certified reference material (molecular formula C12H9ClN2, MW 216.67 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 FormulaC12H9ClN2
Molecular Weight216.67 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Halogen ContentCl-containing
Nitrogen Atoms2

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