Quassin
Title: Quassin
CAS Registry Number: 76-78-8
CAS Name: 2,12-Dimethoxypicrasa-2,12-diene-1,11,16-trione
Additional Names: 3ab,6ab,7,7aa,8,11a,11ba,11c-octahydro-2,10-dimethoxy-3,8a,11ab,11cb-tetramethylphenanthro[10,1-bc]pyran-1,5,11(4H)-trione; nigakilactone D
Molecular Formula: C22H28O6
Molecular Weight: 388.45
Percent Composition: C 68.02%, H 7.27%, O 24.71%
Literature References: One of the bitter constituents of the wood of Quassia amara L., Simaroubaceae known in commerce as Surinam quassia. Obtained by the resolution of the mixture of bitter constituents of quassia wood: E. P. Clark, J. Am. Chem. Soc. 59, 927 (1937); London et al., J. Chem. Soc. 1950, 3431. Structure: Valenta et al., Tetrahedron Lett. no. 20, 25 (1960); Carman, Ward, ibid. 1961, 317; Valenta et al., Tetrahedron 15, 100 (1961). Stereochemistry: Valenta et al., ibid. 18, 1433 (1962). Identity with nigakilactone D: Murae et al., ibid. 27, 1545 (1971). Synthetic approach: Stojanac et al., Can. J. Chem. 53, 619 (1975); P. A. Grieco et al., Tetrahedron Lett. 21, 1619 (1980). Total synthesis of dl-form: eidem, J. Am. Chem. Soc. 102, 7586 (1980).
Properties: Very bitter rectangular plates from dilute methanol, mp 222°. [a]D20 +34.5° (c = 5.09 in CHCl3). uv max: ~255 nm (e ~11,650). Sol in benzene, alc, acetone, chloroform, pyridine, acetic acid, hot ethyl acetate. Sparingly sol in ether, petr ether. Bitterness threshold 1:60,000.
Melting point: mp 222°
Optical Rotation: [a]D20 +34.5° (c = 5.09 in CHCl3)
Absorption maximum: uv max: ~255 nm (e ~11,650)

Others monographs:
Semicarbazide HydrochlorideRimonabantBietanautineLarkspur
Nitrogen PentoxideDiethadioneIridomyrmecinGalangin
PanipenemMethyleneaminoacetonitrilePotassium p-AminobenzoateAstatine
Cizolirtineo-PhthalaldehydeOil of Bitter OrangeBifenthrin
©2016 DrugLead US FDA&EMEA