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Chloroacetophenone oxime

From Wikipedia, the free encyclopedia
Chloroacetophenone oxime
Names
Preferred IUPAC name
(1Z)-2-Chloro-N-hydroxy-1-phenylethan-1-imine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C8H8ClNO/c9-6-8(10-11)7-4-2-1-3-5-7/h1-5,11H,6H2/b10-8-
    Key: VLXDSXLUNPBBOT-NTMALXAHSA-N
  • C1=CC=C(C=C1)C(=NO)CCl
Properties
C8H8ClNO
Molar mass 169.61 g·mol−1
Melting point 88.5–89 °C (191.3–192.2 °F; 361.6–362.1 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Chloroacetophenone oxime is the oxime derivative of chloroacetophenone. It's produced by reaction of chloroacetophenone with hydroxylamine. It has powerful lachrymatory and irritant effects.[1]

References

[edit]
  1. ^ Sartori, Mario (1939). The War Gases. New York: D. Von Nostrand. p. 160.