Weight | 127.958 g/mol |
---|---|
Formula | C2H3Cl2NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
2,2-Dichloroacetamide (683-72-7)
dichloroacetamide
Score:
#5306 in Biology
,
#6984 in Chemistry
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- Dichloroacetamide antidotes enhance thiocarbamate sulfoxide detoxification by elevating corn root glutathione content and glutathione S-transferase activity (Pesticide Biochemistry and Physiology, 1976)
- Precursors of Dichloroacetamide, an Emerging Nitrogenous DBP Formed during Chlorination or Chloramination (Environmental Science & Technology, 2010)
- Dichloroacetonitrile and dichloroacetamide can form independently during chlorination and chloramination of drinking waters, model organic matters, and wastewater effluents. (Environmental Science & Technology, 2012)
- Dichloroacetamide antidotes for thiocarbamate herbicides: mode of action (Science, 1975)
- Comparative vibrational spectroscopic studies, HOMOLUMO and NBO analysis of N-(phenyl)-2,2-dichloroacetamide, N-(2-chloro phenyl)-2,2-dichloroacetamide and N-(4-chloro phenyl)-2,2-dichloroacetamide based on density functional theory (Computational and Theoretical Chemistry, 2013)
- Monensin and dichloroacetamide influences on methane and volatile Fatty Acid production by rumen bacteria in vitro. (Applied and Environmental Microbiology, 1979)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dichloroacetamide
-
SMILESC(C(=O)N)(Cl)Cl
-
InChIKeyWCGGWVOVFQNRRS-UHFFFAOYSA-N
- Pubchem - 2,2-Dichloroacetamide
- Wikipedia - 2,2-dichloroacetamide
Dichloroacetamide is a chlorinated derivative of acetamide.
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