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CAS No 21200-24-8 , (-)-Indolmycin

  • Name: (-)-Indolmycin
  • Synonyms: [5S,(-)]-5-[(R)-1-(1H-Indol-3-yl)ethyl]-2-methylamino-2-oxazolin-4-one;Pa-155-A;(-)-Indolmycin;(S)-5-[(1R)-1-(1H-Indol-3-yl)ethyl]-2-(methylamino)-4(5H)-oxazolone;
  • CAS Registry Number:
  • Flash Point: 208.3°C
  • Boiling Point: 420.8°C at 760 mmHg
  • Density: 1.36g/cm3
  • Refractive index: 1.669
  • Flash Point: 208.3°C
  • Molecular Weight: 0
  • InChI: InChI=1/C14H15N3O2/c1-8(12-13(18)17-14(15-2)19-12)10-7-16-11-6-4-3-5-9(10)11/h3-8,12,16H,1-2H3,(H,15,17,18)/t8-,12+/m1/s1
  • Molecular Formula: C14H15N3O2
  • Molecular Structure:CAS No:21200-24-8 (-)-Indolmycin
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21200-24-8 SC-202183 INDOLMYCIN

  • United States Santa Cruz Biotechnology, Inc. [Manufacturer]
  • Tel: 831-457-3800/ 800-457-3801
  • Fax: 831-457-3801
  • Address: Santa Cruz Biotechnology, Inc.
    2145 Delaware Ave.
    Santa Cruz, CA 95060 null,nullUnited States
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21200-24-8 INDOLMYCIN

  • Germany Cfm Oskar Tropitzsch [Manufacturer]
  • Tel: +49-9231-9619-0
  • Fax: +49-9231-9619-60
  • Address: Cfm Oskar Tropitzsch
    Waldershofer Str. 49-51
    95615 Marktredwitz
    Germany null,nullGermany
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References of (-)-Indolmycin
Title: Indolmycin
CAS Registry Number: 21200-24-8
CAS Name: (5S)-5-[(1R)-1-(1H-Indol-3-yl)ethyl]-2-(methylamino)-4(5H)-oxazolone
Synonyms: (1R,5S)-5-(1-indol-3-ylethyl)-2-(methylamino)-2-oxazolin-4-one; 2-methylamino-5a-(b-indolyl)ethyl-2-oxazolin-4-one
Manufacturers' Codes: PA-155A
Molecular Formula: C14H15N3O2
Molecular Weight: 257.29
Percent Composition: C 65.35%, H 5.88%, N 16.33%, O 12.44%
Literature References: Antibiotic substance produced by Streptomyces albus: Rao, Antibiot. Chemother. 10, 312 (1960); Marsh et al., ibid. 316; GB 862685 (1961 to Pfizer). Structure: M. Schach von Wittenau, H. Els, J. Am. Chem. Soc. 83, 4678 (1961). Total synthesis: eidem, ibid. 85, 3425 (1963); Preobrazhenskaya et al., Tetrahedron 24, 6131 (1968); T. Takeda, T. Mukaiyama, Chem. Lett. 1980, 163. Abs config: T. H. Chan, R. K. Hill, J. Org. Chem. 35, 3519 (1970). Biosynthetic studies: Hornemann et al., Chem. Commun. 1969, 245; eidem, J. Am. Chem. Soc. 93, 3028 (1971).
Properties: Long rectangular prisms from methanol or ethyl acetate, mp 209-210°. [a]D25 -214° (c = 2 in methanol). uv max: 218 nm (E1%1cm 1960). Weakly basic, stable to heat. Slightly sol in water, benzene, ether; moderately in lower alcohols, acetone.
Melting point: mp 209-210°
Optical Rotation: [a]D25 -214° (c = 2 in methanol)
Absorption maximum: uv max: 218 nm (E1%1cm 1960)