| Weight | 190.029 g/mol |
|---|---|
| Formula | C7H5Cl2NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,6-DICHLOROBENZAMIDE (2008-58-4)
Score:
#169 in Environmental science
,
#2756 in Biology
,
#3457 in Chemistry
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- Sorption of the herbicide dichlobenil and the metabolite 2,6-dichlorobenzamide on soils and aquifer sediments (Environmental Science & Technology, 2004)
- Degradation and Mineralization of Nanomolar Concentrations of the Herbicide Dichlobenil and Its Persistent Metabolite 2,6-Dichlorobenzamide by Aminobacter spp. Isolated from Dichlobenil-Treated Soils (Applied and Environmental Microbiology, 2007)
- Mineralisation of 2,6-dichlorobenzamide (BAM) in dichlobenil-exposed soils and isolation of a BAM-mineralising Aminobacter sp. (Environmental Pollution, 2006)
- Toxicity of 2,6-Dichlorothiobenzamide (Chlorthiamid) and 2,6-Dichlorobenzamide in the Olfactory Nasal Mucosa of Mice (Toxicological Sciences, 1991)
- Transformation of the herbicide 2,6-dichlorobenzonitrile to the persistent metabolite 2,6-dichlorobenzamide (BAM) by soil bacteria known to harbour nitrile hydratase or nitrilase (Biodegradation, 2006)
- A quantitative enzyme-linked immunoassay for the detection of 2,6-dichlorobenzamide (BAM), a degradation product of the herbicide dichlobenil. (Journal of Immunological Methods, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C(=C1)Cl)C(=O)N)Cl
-
InChIKeyJHSPCUHPSIUQRB-UHFFFAOYSA-N
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