Acyl chloride

Reactive derivative of carboxylic acids (e.g., used to introduce chloromethyl groups).

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A Convenient Synthesis of 3-Chloromethyl-2(3H)-benzothiazolones
Related Chemicals
- 6-Methyl-3-(p-tolylthiomethyl)-2(3H)-benzothiazolone
Convenient conversion of acid to Weinreb's amide
Related Chemicals
- N-Methoxy-N-MethylcinnaMaMide
Synthesis and properties of di(polyfluoroalkyl) peroxydicarbonates
Related Chemicals
- Carbonochloridic acid, 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoroheptyl ester

Synthesis Column chromatography Melting point Yield NMR spectroscopy Catalyst Solvent reflux Recrystallization Mass spectrometry (MS) Nucleophilic substitution Differential scanning calorimetry (DSC) Stirring TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Vacuum distillation FT-IR spectroscopy Weinreb amide Anhydrous conditions Carboxylic acid Workup Safety Precautions Quenching Radical Initiator Thermogravimetric Analysis (TGA) Stoichiometry Purity Gas chromatography (GC) Oxalyl chloride IR (Infrared Spectroscopy) IR Spectroscopy (Infrared Spectroscopy) DCC (Dicyclohexylcarbodiimide) Activating agent Phase-Transfer Catalyst (PTC)

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