CAS No 37895-35-5 , 1H-Xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione,13-amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-,(1S,4R,8aR)-

Name: 1H-Xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione,13-amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-,(1S,4R,8aR)-
Synonyms: Antibiotic P 42-1;1H-Xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione,13-amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-, [1S-(1a,4a,8aa)]-; Albofungin;1H-Xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione,13-amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-,(1S,4R,8aR)-;
CAS Registry Number:37895-35-5
Flash Point: 479.6°C
Boiling Point: 869.4°Cat760mmHg
Density: 1.71g/cm³
Refractive index: 1.793
Flash Point: 479.6°C
Molecular Weight: 0
InChI: InChI=1/C27H24N2O9/c1-9-5-10-6-11-7-14-18-19(15(11)21(31)16(10)27(34)29(9)28)23(33)26-20(25(18)37-8-36-14)22(32)17-12(30)3-4-13(35-2)24(17)38-26/h5-6,12-14,30-31,33H,3-4,7-8,28H2,1-2H3
Molecular Formula: C27H24 N2 O9
Molecular Structure:

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References of 1H-Xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione,13-amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-,(1S,4R,8aR)-

Title: Albofungin
CAS Registry Number: 37895-35-5
CAS Name: [1S-(1a,4a,8aa)]-13-Amino-3,4,8a,13-tetrahydro-1,15,16-trihydroxy-4-methoxy-12-methyl-1H-xantheno[4￠,3￠,2￠:4,5][1,3]benzodioxino[7,6-g]isoquinoline-14,17(2H,9H)-dione
Molecular Formula: C27H24N2O9
Molecular Weight: 520.49
Percent Composition: C 62.30%, H 4.65%, N 5.38%, O 27.67%
Literature References: Antifungal antibiotic produced by Streptomyces albus var fungistaticus (fungatus) Solovyeva et Rudaya. Isoln procedure: Khokhlov, Liberman, Proc. Symp. Antibiotics Prague (May 1959) p 81. Structure: A. I. Gurevich et al., Tetrahedron Lett. 1972, 1751. Stereochemistry: A. I. Gurevich et al., ibid. 1974, 2801. Thought to be identical with Ba-180265 described by Liu et al., in Antimicrob. Agents Chemother. 1962, 767. Chemical and biological properties: A.I. Gurevich et al., Antibiotiki 17, 771 (1972).
Properties: Crystals from nitromethane, mp 304-307°. Also reported as mp 190° (dec). [a]D20 -670° (DMF). uv max (ethanol): 228, 254, 303, 376 nm (log e 4.58, 4.58, 4.19, 4.42). Practically insol in water, petr ether. Sparingly sol in alcohol; quite sol in chloroform, dichloroethane, acetone, chlorobenzene, formamide, dimethylformamide, glacial acetic acid.
Melting point: mp 304-307°; mp 190° (dec)
Optical Rotation: [a]D20 -670° (DMF)
Absorption maximum: uv max (ethanol): 228, 254, 303, 376 nm (log e 4.58, 4.58, 4.19, 4.42)