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CAS No 3690-12-8 , 4-Amino-2-methoxy-5-pyrimidinemethanol

  • Name: 4-Amino-2-methoxy-5-pyrimidinemethanol
  • Synonyms: 4-Amino-5-(hydroxymethyl)-2-methoxypyrimidine;4-Amino-2-methoxy-5-pyrimidylmethanol;NSC 66577;4-Amino-2-methoxy-5-pyrimidinemethanol;Bacimethrin;5-Pyrimidinemethanol,4-amino-2-methoxy-;Bacimethrine;Bacimetrin;
  • CAS Registry Number:
  • Flash Point: 192.7 °C
  • Boiling Point: 394.9 °Cat760mmHg
  • Density: 1.337 g/cm3
  • Refractive index: 1.602
  • Flash Point: 192.7 °C
  • Molecular Weight: 155.1
  • InChI: InChI=1/C6H9N3O2/c1-11-6-8-2-4(3-10)5(7)9-6/h2,10H,3H2,1H3,(H2,7,8,9)
  • Molecular Formula: C6H9N3O2
  • Molecular Structure:CAS No:3690-12-8 4-Amino-2-methoxy-5-pyrimidinemethanol

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3690-12-8 4-Amino-2-methoxy-5-pyrimidinemethanol

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3690-12-8 4-Amino-2-methoxy-5-pyrimidinemethanol

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References of 4-Amino-2-methoxy-5-pyrimidinemethanol
Title: Bacimethrin
CAS Registry Number: 3690-12-8
CAS Name: 4-Amino-2-methoxy-5-pyrimidinemethanol
Synonyms: 4-amino-5-hydroxymethyl-2-methoxypyrimidine
Molecular Formula: C6H9N3O2
Molecular Weight: 155.15
Percent Composition: C 46.45%, H 5.85%, N 27.08%, O 20.62%
Literature References: Antibiotic substance produced by Bacillus megatherium from Japanese soil. Isoln and structure: F. Tanaka et al., J. Antibiot. 14A, 161 (1961); 15A, 191, 197 (1962). Prepn: GB 884772 (1961 to Merck & Co.); Koppel et al., J. Org. Chem. 27, 1492, 3614 (1962). Biological studies: T. Nishimura, N. Tanaka, J. Antibiot. 16A, 179 (1963).
Properties: Needles from methanol, or ethanol + ether, mp 174°. uv max (water): 227, 271 nm (e 7600, 7300); (0.1N HCl): 229, 261 nm (e 8400, 9500). Sol in water, methanol, acetic acid. Mod sol in ethanol, pyridine. Practically insol in other organic solvents. LD50 in mice (mg/kg): 300 i.v., 300 i.p (Tanaka, p 191).
Melting point: mp 174°
Absorption maximum: uv max (water): 227, 271 nm (e 7600, 7300); (0.1N HCl): 229, 261 nm (e 8400, 9500)
Toxicity data: LD50 in mice (mg/kg): 300 i.v., 300 i.p (Tanaka, p 191)
 
 
Status: This monograph has been retired and is no longer subject to revision or update.