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Names | |
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Preferred IUPAC name
(1Z)-2-Chloro-N-hydroxy-1-phenylethan-1-imine | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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CompTox Dashboard (
EPA)
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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]
![]() | |
Names | |
---|---|
Preferred IUPAC name
(1Z)-2-Chloro-N-hydroxy-1-phenylethan-1-imine | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
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]