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CAS No 59-06-3 , methyl 4-acetamido-2-ethoxybenzoate

  • Name: methyl 4-acetamido-2-ethoxybenzoate
  • Synonyms: Ethopabat; EINECS 200-414-3;Methyl 4-acetamido-2-ethoxybenzoate; NCGC00160624-01; 4-Acetamido-2-ethoxybenzoesaeuremethylester;methyl 4-acetamido-2-ethoxybenzoate; 59-06-3;
  • CAS Registry Number:
  • Density: 1.18 g/cm3
  • Refractive index: 1.545
  • Safety Statements: R22
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 200-414-3
  • Molecular Weight: 237.2518
  • InchiKey: GOVWOKSKFSBNGD-UHFFFAOYSA-N
  • InChI: InChI=1S/C12H15NO4/c1-4-17-11-7-9(13-8(2)14)5-6-10(11)12(15)16-3/h5-7H,
    4H2,1-3H3,(H,13,14)
  • Risk Statements: R22
  • Molecular Formula: C12H15NO4
  • Molecular Structure:CAS No:59-06-3 methyl 4-acetamido-2-ethoxybenzoate

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59-06-3 Methyl 4-acetamido-2-ethoxybenzoate

  • Chemical Name: Methyl 4-acetamido-2-ethoxybenzoate Chemical Type: Pharma Intermediates Catalog No: AC-10126 CASNO: 59-06-3 Molecular Formula: C12H15NO4 Molecular Weight: 237.25 Purity: 98% welcome: sales(at)achemo(dot)com
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References of methyl 4-acetamido-2-ethoxybenzoate
Title: Ethopabate
CAS Registry Number: 59-06-3
CAS Name: 4-Acetamido-2-ethoxybenzoic acid methyl ester
Synonyms: methyl 4-acetamido-2-ethoxybenzoate; 2-ethoxy-4-acetamidobenzoic acid methyl ester; ethyl pabate
Molecular Formula: C12H15NO4
Molecular Weight: 237.25
Percent Composition: C 60.75%, H 6.37%, N 5.90%, O 26.97%
Literature References: Prepn: Grimme, Schmitz, Ber. 87, 179 (1954); E. F. Rogers, R. L. Clark, BE 613166; eidem, US 3211610 (1962, 1965 both to Merck & Co.); FR 1407055; M. L. Thominet, US 3357978 (1965, 1967 both to Soc. d'Etudes Sci. Ind. de l'Ile-de-France). Anticoccidial activity studies: Rogers et al., Proc. Soc. Exp. Biol. Med. 117, 488 (1964). Metabolism in chickens: Buhs et al., J. Pharmacol. Exp. Ther. 154, 357 (1966).
Properties: White to pinkish-white, practically odorless crystals from methanol and water, mp 148-149°. uv max (methanol): 298, 267 nm (A1%1cm 805, 365). Sol in methanol, ethanol, acetone, acetonitrile. Sparingly sol in isopropanol, p-dioxane, ethyl acetate, methylene chloride; very slightly sol in water and isooctane.
Melting point: mp 148-149°
Absorption maximum: uv max (methanol): 298, 267 nm (A1%1cm 805, 365)
 
Derivative Type: Mixture with amprolium
Trademarks: Amprol Plus (Merck & Co.)
 
Therap-Cat-Vet: Mixture as coccidiostat.