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CAS No 37764-25-3 , 2,2-dichloro-N,N-bis(prop-2-enyl)acetamide

  • Name: 2,2-dichloro-N,N-bis(prop-2-enyl)acetamide
  • Synonyms: Compound R-25788;2,2-dichloro-N,N-bis(prop-2-enyl)acetamide; Dichloromid; Stauffer R-25788; 37764-25-3; N,N-DIALLYL-2,2-DICHLOROACETAMIDE;N,N-Diallyldichloroacetamide;
  • CAS Registry Number:
  • Melting Point: 5.0-6.5 ºC
  • Density: 1.192-1.204
  • Refractive index: 1.494
  • Water Solubility: In water
  • Safety Statements: Moderately toxic by ingestion. When heated to decomposition it emits very toxic fumes of Cl− and NOx. See also ALLYL COMPOUNDS.
  • Hazard Symbols: Xi: Irritant;N: Dangerous for the environment;
  • EINECS: 253-658-8
  • Molecular Weight: 208.08504
  • InchiKey: YRMLFORXOOIJDR-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H11Cl2NO/c1-3-5-11(6-4-2)8(12)7(9)10/h3-4,7H,1-2,5-6H2
  • Risk Statements: R43; R50/53
  • Molecular Formula: C8H11Cl2NO
  • Molecular Structure:CAS No:37764-25-3 2,2-dichloro-N,N-bis(prop-2-enyl)acetamide

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  • Dichlormid Name: Dichlormid Synonyms: Dichlormid ,EPTC antidote, R-25788,Antidote dichlormid,Dichlormid safener eradicane;, N,N-Diallyl-2,2-dichloroacetamide CAS NO:37764-25-3 EINECS: 253-658-8 Structural formula:C8H11Cl2NO
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References of 2,2-dichloro-N,N-bis(prop-2-enyl)acetamide
Title: Dichlormid
CAS Registry Number: 37764-25-3
CAS Name: 2,2-Dichloro-N,N-di-2-propenylacetamide
Synonyms: 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.