Explore: Chloropropionyl Chloride
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Books Results
Source: The Open Library
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1Relative rates of the aluminium chloride-catalysed reactions of methylbenzenes with 3-chloropropionyl chloride in ethylene dichloride
By Pentti Olavi Ilmari Virtanen
“Relative rates of the aluminium chloride-catalysed reactions of methylbenzenes with 3-chloropropionyl chloride in ethylene dichloride” Metadata:
- Title: ➤ Relative rates of the aluminium chloride-catalysed reactions of methylbenzenes with 3-chloropropionyl chloride in ethylene dichloride
- Author: Pentti Olavi Ilmari Virtanen
- Language: English
- Number of Pages: Median: 16
- Publisher: Suomalainen tiedeakatemia
- Publish Date: 1968
- Publish Location: Helsinki
“Relative rates of the aluminium chloride-catalysed reactions of methylbenzenes with 3-chloropropionyl chloride in ethylene dichloride” Subjects and Themes:
- Subjects: Aluminum chloride - Chemical kinetics - Chloropropionyl chloride - Toluene
Edition Identifiers:
- The Open Library ID: OL4622089M
- Library of Congress Control Number (LCCN): 77453021
Access and General Info:
- First Year Published: 1968
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
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Wiki
Source: Wikipedia
Wikipedia Results
Search Results from Wikipedia
2-Chloropropionic acid
is produced by chlorination of propionyl chloride followed by hydrolysis of the 2-chloropropionyl chloride. Enantiomerically pure (S)-2-chloropropionic
Halohydrin
is produced by chlorination of propionyl chloride followed by hydrolysis of the 2-chloropropionyl chloride. Enantiomerically pure (S)-2-chloropropionic
Ethacizine
between Phenothiazine-2-ethylcarbamate [37711-29-8] (1) and 3-Chloropropionyl chloride [625-36-5] (2) gives ethyl N-[10-(3-chloropropanoyl)phenothiazin-2-yl]carbamate
Moracizine
forms the phenothiazine derivative (4). Amide formation with 3-chloropropionyl chloride (5) gives the penultimate intermediate (6). Alkylation of morpholine
Α,N,N-Trimethyltryptamine
treated first with PBr3 followed by dimethylamine. Or, reaction with chloropropionyl chloride gave a 1,3-bis intermediate which was converted to the amino ketone