4-(4-Chlorophenyl)-N-2-propen-1-yl-2-thiazolamine CAS 21344-79-6

Purity 97%+In StockPharmaceutical Standards
CAS No.21344-79-6
Molecular FormulaC12H11ClN2S
Molecular Weight250.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Chlorophenyl)-N-2-propen-1-yl-2-thiazolamine CAS 21344-79-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 250.75 g/mol gives 4-(4-Chlorophenyl)-N-2-propen-1-yl-2-thiazolamine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(4-Chlorophenyl)-N-2-propen-1-yl-2-thiazolamine (CAS 21344-79-6) is a high-purity analytical reference standard with the molecular formula C12H11ClN2S and a molecular weight of 250.75 g/mol.

Based on its molecular formula C12H11ClN2S, 4-(4-Chlorophenyl)-N-2-propen-1-yl-2-thiazolamine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 250.75 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC12H11ClN2S
Molecular Weight250.75 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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