4-chlorobenzyl chloride
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 4-chlorobenzyl chloride | |||||||||||||||
other names |
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Molecular formula | C 7 H 6 Cl 2 | |||||||||||||||
Brief description |
colorless to yellowish solid with a pungent odor |
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properties | ||||||||||||||||
Molar mass | 161.03 g mol −1 | |||||||||||||||
Physical state |
firmly |
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density |
1.27 g cm −3 (20 ° C) |
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Melting point |
27 ° C |
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boiling point |
220.6 ° C |
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Vapor pressure |
1.5 h Pa (50 ° C) |
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solubility |
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safety instructions | ||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
4-chlorobenzyl chloride is a chemical compound and a derivative of benzyl chloride . It can by chlorination of 4-chlorotoluene are obtained.
use
4-chlorobenzyl chloride is required for the synthesis of pesticides such as chlorine surfactant.
Individual evidence
- ↑ a b c d e f g Entry on alpha, 4-dichlorotoluene in the GESTIS substance database of the IFA , accessed on January 8, 2018(JavaScript required) .
- ↑ a b c C. Loring Jackson, Alfred W. Field: Ueber Parachlorbenzylchlorid and its derivatives . In: Reports of the German Chemical Society . tape 11 , no. 1 , January 1878, p. 904-905 , doi : 10.1002 / cber.187801101243 ( PDF ).
- ↑ Radical substitution of p-chlorotoluene to p-chlorobenzyl chloride
- ↑ Entry on 4-chlorobenzyl chloride in the Hazardous Substances Data Bank , accessed on July 12, 2016.
- ↑ Thomas A. Unger: Pesticide Synthesis Handbook . William Andrew, 1996, ISBN 0-8155-1853-6 , pp. 1029 ( limited preview in Google Book search).