5-Methyl-1,2,3-oxadiazole-4-carbonyl chloride CAS 914637-79-9

Purity 97%+In StockPharmaceutical Standards
CAS No.914637-79-9
Molecular FormulaC4H3ClN2O2
Molecular Weight146.53 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Methyl-1,2,3-oxadiazole-4-carbonyl chloride CAS 914637-79-9 chemical structure

Description

As a certified reference material (CRM), 5-Methyl-1,2,3-oxadiazole-4-carbonyl chloride 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.

5-Methyl-1,2,3-oxadiazole-4-carbonyl chloride (CAS 914637-79-9), molecular formula C4H3ClN2O2 and molecular weight 146.53 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 5-Methyl-1,2,3-oxadiazole-4-carbonyl chloride (C4H3ClN2O2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 146.53 g/mol, it falls into the low-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC4H3ClN2O2
Molecular Weight146.53 g/mol
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)4.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2

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