1'-Methyl-6',7',8',9'-tetrahydrospiro[cyclohexane-1,5'-thiazolo[3,2-a]quinazoline] hydrobromide CAS 21457-11-4

Purity 97%+In StockPharmaceutical Standards
CAS No.21457-11-4
Molecular FormulaC16H22N2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1'-Methyl-6',7',8',9'-tetrahydrospiro[cyclohexane-1,5'-thiazolo[3,2-a]quinazoline] hydrobromide CAS 21457-11-4 chemical structure

Description

CATO supplies 1'-Methyl-6',7',8',9'-tetrahydrospiro[cyclohexane-1,5'-thiazolo[3,2-a]quinazoline] hydrobromide (CAS 21457-11-4), a certified reference material (molecular formula C16H22N2SHBr, MW 355.34 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H22N2SHBr, 1'-Methyl-6',7',8',9'-tetrahydrospiro[cyclohexane-1,5'-thiazolo[3,2-a]quinazoline] hydrobromide contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 355.34 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

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 FormulaC16H22N2S HBr
Molecular Weight355.34 g/mol
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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