Weight | 173.643 g/mol |
---|---|
Formula | C8H12ClNO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
Allidochlor (93-71-0)
CDAA · Randox · 2-chloro-N,N-diallylacetamide
Score:
#2314 in Biology
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#2864 in Chemistry
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- Mercapturic acid formation in the metabolism of propachlor, CDAA, and fluorodifen in the rat (Pesticide Biochemistry and Physiology, 1975)
- Effect of Chinese medicines Chan Su and Danshen on EMIT 2000 and Randox digoxin immunoassays: wide variation in digoxin-like immunoreactivity and magnitude of interference in digoxin measurement by different brands of the same product. (Therapeutic Drug Monitoring, 2002)
- Validation of the only commercially available immunoassay for synthetic cathinones in urine: Randox Drugs of Abuse V Biochip Array Technology (Drug Testing and Analysis, 2014)
- The effect of CDAA (N,N,-diallyl-2-chloroacetamide) pretreatments on subsequent CDAA injury to corn (Zea mays L.) (Pesticide Biochemistry and Physiology, 1985)
- Biochemical Action of CDAA, a New Herbicide (Science, 1956)
- Antioxidant capacity of seminal plasma measured by TAS Randox. (2007)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - CDAA
- Randox
- 2-chloro-N,N-diallylacetamide
-
SMILESC=CCN(CC=C)C(=O)CCl
-
InChIKeyMDBGGTQNNUOQRC-UHFFFAOYSA-N
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