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CAS No 2751-09-9 , Oleandomycin,2'',4',11-triacetate Search by region : Germany

  • Name: Oleandomycin,2'',4',11-triacetate
  • Synonyms: Oleandomycin,2'',4',11-triacetate; TAO(pharmaceutical); Oleandomycin, triacetate (ester) (8CI,9CI); NSC 108166; Oleandomycin triacetyl ester;Wytrion; Oxiraneheptanoicacid, 2-(3,5-dihydroxy-2,4-dimethylhexanoyl)-d-[[4-(dimethylamino)tetrahydro-3-hydroxy-6-methylpyran-2-yl]oxy]-a,g,e-trimethyl-b-[(tetrahydro-5-hydroxy-4-methoxy-6-methylpyran-2-yl)oxy]-,m-lactone, triacetate (7CI); Oleomycin; Troleandomycin;Oleandomycintriacetate (6CI);Evramycin; Evramicina; Cyclamycin; Wy 651;1,9-Dioxaspiro[2.13]hexadecane, oleandomycin deriv.; Triacetyloleandomycin; Triocetin; TAO;
  • CAS Registry Number:
  • Flash Point: 445.2°C
  • Boiling Point: 812.5°Cat760mmHg
  • Density: 1.19g/cm3
  • Refractive index: 1.515
  • Safety Statements:
    Safety Statements 22-24/25
    WGK Germany 2
    RTECS RJ9900000
    F 8
  • Flash Point: 445.2°C
  • EINECS: 220-392-9
  • Molecular Weight: 813.97
  • InChI: InChI=1/C41H67NO15/c1-19-17-41(18-49-41)38(46)23(5)34(53-27(9)43)21(3)25(7)52-39(47)24(6)35(56-32-16-31(48-14)36(26(8)51-32)54-28(10)44)22(4)33(19)57-40-37(55-29(11)45)30(42(12)13)15-20(2)50-40/h19-26,30-37,40H,15-18H2,1-14H3
  • Molecular Formula: C41H67 N O15
  • Molecular Structure:CAS No:2751-09-9 Oleandomycin,2'',4',11-triacetate

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2751-09-9 TROLEANDOMYCIN

  • Germany BIOTREND Chemikalien GmbH [Manufacturer]
  • Tel: ++49 (0)2 21 9 49 83 20
  • Fax: ++49 (0)2 21 9 49 83 25
  • Address: BIOTREND Chemikalien GmbH
    Eupener Str. 157
    D - 50933 Cologne
    Germany null,nullGermany
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References of Oleandomycin,2'',4',11-triacetate
Title: Troleandomycin
CAS Registry Number: 2751-09-9
CAS Name: Oleandomycin triacetate ester
Synonyms: triacetyloleandomycin
Manufacturers' Codes: NSC-108166
Trademarks: Cyclamycin (Wyeth); Wytrion (Wyeth); Evramycin (Wyeth); TAO (Roerig); Triocetin (OFF)
Molecular Formula: C41H67NO15
Molecular Weight: 813.97
Percent Composition: C 60.50%, H 8.30%, N 1.72%, O 29.48%
Literature References: Semi-synthetic macrolide antibiotic. Prepd from oleandomycin: Celmer et al., Antibiot. Annu. 1957-1958, p 476; GB 877730 (1958 to Pfizer); M. Khristov, N. Petkov, Farmatsiya (Sofia) 27, 1 (1977), C.A. 90, 23458c (1979). Review: S. Ross, Antimicrobial Therapy, B. M. Kagan, Ed. (Saunders, Philadelphia, 1970) pp 134-144.
Properties: Crystals from isopropanol. Practically tasteless. Dec 176°. [a]D25 -23° (methanol). pKa 6.6. Soly in water <0.1 g/100 ml.
pKa: pKa 6.6
Optical Rotation: [a]D25 -23° (methanol)
Therap-Cat: Antibacterial.
Keywords: Antibacterial (Antibiotics); Macrolides.