Dichlormid
Structural Formula Vector Image
Title: Dichlormid
CAS Registry Number: 37764-25-3
CAS Name: 2,2-Dichloro-N,N-di-2-propenylacetamide
Additional Names: N,N-diallyl-2,2-dichloroacetamide
Manufacturers' Codes: R-25788
Molecular Formula: C8H11Cl2NO
Molecular Weight: 208.09
Percent Composition: C 46.18%, H 5.33%, Cl 34.07%, N 6.73%, O 7.69%
Literature References: Increases corn tolerance to thiocarbamate and chloroacetanilide herbicides. Field and growth room trials in protection of corn from herbicide injury: F. Y. Chang et al., Can. J. Plant Sci. 52, 707 (1972); eidem, Weed Res. 13, 399 (1973). Effects on uptake and metabolism of EPTC, q.v.: eidem, J. Agric. Food Chem. 22, 245 (1974). Prepn and use in combination with thiocarbamate herbicides: F. M. Pallos et al., US 4021224 (1977 to Stauffer). Synergistic activity with herbicides that affect photosynthesis: C. Fedtke, R. H. Strang, Z. Naturforsch. 45c, 565 (1990). Effects on lipid biosynthesis in maize: I. Cs. Barta, ibid. 46c, 926 (1991); in barley and wild oats: A. Baldwin et al., J. Exp. Bot. 54, 1289 (2003). Environmental tolerances: Fed. Regist. 65, 16143 (2000). Photodegradation study: A. W. Abu-Qare, H. J. Duncan, Chemosphere 46, 1183 (2002).
Properties: bp0.4 kPa 96°. nD30 1.4990. LD50 orally in rats: 2146 mg/kg (Fed. Regist.).
Boiling point: bp0.4 kPa 96°
Index of refraction: nD30 1.4990
Toxicity data: LD50 orally in rats: 2146 mg/kg (Fed. Regist.)
 
Derivative Type: Combination with acetochlor
CAS Registry Number: 144115-48-0
Trademarks: Surpass (Dow AgroSci.); TopNotch (Dow AgroSci.)
 
Use: Herbicide safener.

Other Monographs:
Catechu BlackMelanostatinAurinPentoxifylline
Diamthazole DihydrochlorideFlavoxanthinCerous Chloride4,4'-Dinitrocarbanilide
CyclovalonePotassium PyrosulfateScammony RootCarisoprodol
OxidimethiinChromium DioxideTroxipideMikamycin
©2006-2023 DrugFuture->Chemical Index Database