683-50-1

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 272, 1962 DOI: 10.1021/jo01048a066

InChI:InChI=1/C3H5ClO/c1-3(4)2-5/h2-3H,1H3

Upstream product

• 71-23-8 propan-1-ol 
• 116435-96-2 1,2-dichloro-1-propoxy-propane 
• 7732-18-5 water 
• 123-38-6 propionaldehyde 

Downstream Products

• 3581-89-3 5-methylthiazole 
• 7305-71-7 5-methyl-2-thiazol-2-amine 
• 25362-06-5 Dimethyl trans-1-propenylphosphonate 
• 592-20-1 Acetol acetate 
• 55712-50-0 phosphoric acid dimethyl ester propenyl ester 
• 121788-93-0 3-Chlor-1-phenyl-2-(trimethylsiloxy)-1-butanon 
• 116171-34-7 2-(1-phenylhydrazino)-1-propanone phenylhydrazone 
• 51828-58-1 2-(4-Chloro-phenylsulfanyl)-propionaldehyde 
• 1186130-47-1 C₁₈H₂₁NO₆ 
• 1186130-53-9 C₁₇H₁₉NO₆ 
• 1186130-50-6 C₁₇H₁₉NO₆ 
• 55064-96-5 2-(phenylthio)propanal 
• 42046-68-4 3-cyano-5-methyl-pyrrole-2-carboxylic acid 
• 67856-03-5 5-methyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diol 

Relevant academic research and scientific papers

METHOD FOR PRODUCING 3,3,3-TRIFLUOROPROPIONIC ACID CHLORIDE

There is provided a process for producing 3,3,3-trifluoropropionyl chloride, which is characterized in that 3,3,3-trifluoropropionaldehyde is chlorinated by a chlorinating agent selected from the group consisting of chlorine (Cl2), sulfuryl chloride (SO2Cl2) and organic N-chloro compounds.

Kinetics of Oxidation of Methanol, Ethanol and n-Propanol by t-Butyl Hypochlorite

The kinetics of oxidation of ethanol (methanol or n-propanol) with t-BuOCl have been investigated at 40 deg C.The order of reaction is one each with respect to ethanol and t-BuOCl.The effect of ionic strength, and various metallic chlorides on the reaction rate has been studied.The various activation parameters have been evaluated.A mechanism involving ester formation is proposed.