| Weight | 155.584 g/mol |
|---|---|
| Formula | C7H6ClNO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Chlorobenzamide (618-48-4)
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- The Selective 7 Nicotinic Acetylcholine Receptor Agonist PNU-282987 [N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-4-chlorobenzamide Hydrochloride] Enhances GABAergic Synaptic Activity in Brain Slices and Restores Auditory Gating Deficits in Anesthetized Rats (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Development of Potent Serotonin-3 (5-HT3) Receptor Antagonists. I. Structure-Activity Relationships of 2-Alkoxy-4-amino-5-chlorobenzamide Derivatives. (Chemical & Pharmaceutical Bulletin, 1995)
- Synthesis and Nicotinic Receptor Activity of Chemical Space Analogues of N-(3R)-1-Azabicyclo[2.2.2]oct-3-yl-4-chlorobenzamide (PNU-282,987) and 1,4-Diazabicyclo[3.2.2]nonane-4-carboxylic Acid 4-Bromophenyl Ester (SSR180711) (Journal of Medicinal Chemistry, 2012)
- The Formation of 2-Chlorobenzamide upon Hydrolysis of the Benzoylphenylurea Insecticide 1-(2-Chlorobenzoyl)-3-(4-chlorophenyl) Urea in Different Water Systems (Journal of Agricultural and Food Chemistry, 2001)
- Influence of some biologically active compounds on microbial activity and on the availability of plant nutrients in soils. II. Nitrapyrin, dazomet, 2-chlorobenzamide and tributyl-3-chlorobenzylammonium bromide (Pesticide Science, 1975)
- The (3 + 1)-dimensional superspace description of the commensurately modulated structure of p-chlorobenzamide (-form) and its relation to the -form (Zeitschrift Fur Kristallographie, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)Cl)C(=O)N
-
InChIKeyMJTGQALMWUUPQM-UHFFFAOYSA-N
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