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CAS No 32809-16-8 , 3-(3,5-dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione Search by region : China

  • Name: 3-(3,5-dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione
  • Synonyms: Procymidone [BSI:ISO]; Sumisclex; Sumilex; 32809-16-8;Dicyclidine;3-(3,5-dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione; 3-(3,5-Dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione;
  • CAS Registry Number:
  • Melting Point: 166-167 ºC
  • Boiling Point: 477.9 ºC at 760 mmHg
  • Density: 1.502 g/cm3
  • Refractive index: 1.643
  • Safety Statements: Moderately toxic by intraperitoneal route. Mildly toxic by ingestion and skin contact. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cl− and NOx.
  • EINECS: 251-233-1
  • Molecular Weight: 284.13794
  • InchiKey: QXJKBPAVAHBARF-UHFFFAOYSA-N
  • InChI: InChI=1S/C13H11Cl2NO2/c1-12-6-13(12,
    2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3
  • Molecular Formula: C13H11Cl2NO2
  • Molecular Structure:CAS No:32809-16-8 3-(3,5-dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione

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References of 3-(3,5-dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione
Title: Procymidone
CAS Registry Number: 32809-16-8
CAS Name: 3-(3,5-Dichlorophenyl)-1,5-dimethyl-3-azabicyclo[3.1.0]hexane-2,4-dione
Synonyms: N-(3,5-dichlorophenyl)-1,2-dimethyl-1,2-cyclopropanedicarboximide; dicyclidine
Manufacturers' Codes: S-7131
Trademarks: Sumisclex (Sumitomo); Sumilex (Sumitomo)
Molecular Formula: C13H11Cl2NO2
Molecular Weight: 284.14
Percent Composition: C 54.95%, H 3.90%, Cl 24.95%, N 4.93%, O 11.26%
Literature References: Dicarboximide fungicide systemically active against Botrytis and Sclerotinia spp. on fruits and vegetables. Prepn: NL 7003836; A. Fujinami et al., US 3903090 (1970, 1975 both to Sumitomo). Antimicrobial spectrum and systemic activity: Y. Hisada et al., J. Pestic. Sci. 1, 145 (1976). Mechanism of action: A. C. Pappas, D. J. Fisher, Pestic. Sci. 10, 239 (1979). Field evaluation: I. F. Jackson, B. N. Smith, Proc. 32nd N.Z. Weed Pest Control Conf. 278 (1979). HPLC determn in wine musts and extracts: P. Cabras et al., J. Chromatogr. 256, 176 (1983). Review: N. Mikami, J. Miyamoto, Rev. Plant Prot. Res. 14, 85-95 (1981).
Properties: Crystalline solid, mp 165-167°. d25 1.42-1.46. Vapor pressure: 1.32′10-4 mm Hg. uv max: 207.5, 275 nm (e 4.2′104, 4.1′102). Soly in water (25°): 4.5 ppm. Highly sol in acetonitrile, acetone, ether, chloroform. Moderately sol in benzene, toluene. Stable in solvents. Unstable in alkaline media. LD50 in male rats (mg/kg): 6800 orally, >10000 dermally (Jackson). Also reported as LD50 in male, female rats (g/kg): 7.8, 9.1 orally (Mikami).
Melting point: mp 165-167°
Absorption maximum: uv max: 207.5, 275 nm (e 4.2′104, 4.1′102)
Density: d25 1.42-1.46
Toxicity data: LD50 in male rats (mg/kg): 6800 orally, >10000 dermally (Jackson); LD50 in male, female rats (g/kg): 7.8, 9.1 orally (Mikami)
Use: Systemic agricultural fungicide.