Home > Name List By 2 > 2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic acid

CAS No 81335-37-7 , 2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic
acid

  • Name: 2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic
    acid
  • Synonyms: HSDB 6677; Imazaquin [BSI:ISO]; Imazaquine [ISO-French]; Caswell No. 003C; 81335-37-7;Scepter Herbicide;2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic
    acid;
  • CAS Registry Number:
  • Melting Point: 219-224 ºC
  • Density: 1.35 g/cm3
  • Refractive index: 1.662
  • Safety Statements: Moderately toxic by ingestion and skin contact. Low toxicity by inhalation. When heated to decomposition it emits toxic vapors of NOx.
  • Hazard Symbols: Moderately toxic by ingestion and skin contact. Low toxicity by inhalation.
  • Molecular Weight: 311.33518
  • InchiKey: CABMTIJINOIHOD-UHFFFAOYSA-N
  • InChI: InChI=1S/C17H17N3O3/c1-9(2)17(3)16(23)19-14(20-17)13-11(15(21)22)8-10-6-
    4-5-7-12(10)18-13/h4-9H,1-3H3,(H,21,22)(H,19,20,23)
  • Risk Statements: 21
  • Molecular Formula: C17H17N3O3
  • Molecular Structure:CAS No:81335-37-7 2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic<br />acid

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References of 2-(4-methyl-5-oxo-4-propan-2-yl-1H-imidazol-2-yl)quinoline-3-carboxylic
acid
Title: Imazaquin
CAS Registry Number: 81335-37-7
CAS Name: 2-[4,5-Dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-3-quinolinecarboxylic acid
Synonyms: 2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid
Manufacturers' Codes: AC-252214
Molecular Formula: C17H17N3O3
Molecular Weight: 311.34
Percent Composition: C 65.58%, H 5.50%, N 13.50%, O 15.42%
Literature References: Pre- and post-emergence imidazolinone herbicide especially for use in soybean crops. Prepn: M. Los, EP 41623 (1981 to Am. Cyanamid), C.A. 96, 199687q (1982). Alternate prepn: D. R. Maulding, R. F. Doehner, Jr., US 4459408 (1984 to Am. Cyanamid). Inhibition of branched-chain amino acid biosynthesis: D. L. Shaner et al., Plant Physiol. 76, 545 (1984). Metabolism by plants: D. L. Shaner, P. A. Robson, Weed Sci. 33, 469 (1985). Persistence in soil: G. Basham et al., ibid. 35, 576 (1987). Herbicidal activity: M. W. Beale et al., Proc. Annu. Meet. Northeast. Weed Sci. Soc. 38, 36 (1984); W. F. Congleton et al., Weed Technol. 1, 186 (1987).
Properties: Crystals from hexane + ethyl acetate, mp 219-222° (dec). Slightly sol in some organic solvents. Soly in water at 25°: 60-120 ppm. LD50 orally in rats: 5000 mg/kg; LC50 (96 hr) in rainbow trout: 100 mg/l (Congleton).
Melting point: mp 219-222° (dec)
Toxicity data: LD50 orally in rats: 5000 mg/kg; LC50 (96 hr) in rainbow trout: 100 mg/l (Congleton)
 
Derivative Type: Ammonium salt
Trademarks: Scepter (BASF)
Molecular Formula: C17H20N4O3
Molecular Weight: 328.37
Percent Composition: C 62.18%, H 6.14%, N 17.06%, O 14.62%
Properties: Sol in water.
 
Use: Herbicide.