Ε, Miscellaneous Benzenoids
TABLE 3.1—continued
117
Text
mp
no.
Name
(in degrees)
Reference
61
2,7-Dihydroxy-6-acetyljuglone
215
Moore et al (1966a)
(dec)
62
2,3,7-Trihydroxy-6-acetyljuglone
245-255
Moore et al. (1966a)
(subl.)
63a
8-Hydroxy-5,6-dimethoxy-2-methyl> 200
Kent et al. (1970)
4//-naphtho[2,3-6]pyran-4-one
(dec)
(comantherin) sodium sulfate
67
5,8-Dihy droxy-10-methoxy-2-«232-233
Smith and Sutherland
propyl-4#-naphtho[l ,2-b]pyran(dec)
(1971)
4-one (comaparvin)
68
6- M ethoxyco mapar vin
200-201.5
Smith and Sutherland
(dec)
(1971)
69
6-Methoxycomaparvin 5-methyl
221-222
Smith and Sutherland
ether
(dec)
(1971)
72
1,3-Dihydroxy-6,8-dimethoxy-4208.5-209
Sutherland and Wells
butyryl-9,10-anthraquinone
229.5-230.5
(1967)
(rhodocomatulin 6,8-dimethyl
ether)
74
1,3,8-Trihydroxy-6-methoxy-4250-252
Sutherland and Wells
butyryl-9,1O-anthraquinone
(dec)
(1967)
(rhodocomatulin 6-methyl ether)
75
1,4,5,7-Tetrahydroxy-2-methoxy298-299
Sutherland and Wells
8-butyryl-9,10-anthraquinone
(1967)
(rubrocomatulin 2-methyl ether)
76
l,6,8-Trihydroxy-3-(l-hydroxy217-218
Powell and Sutherland
propyl)-9,10-anthraquinone
(1967b)
(rhodoptilometrin)
77
1,6,8-Trihydroxy-3-(2-hydroxy275-277
Powell and Sutherland
propyl)9,10-anthraquinone
(1967b)
(isorhodoptilometrin)
78
1,6,8-Trihydroxy-3-propyl-9,10298-299
Powell and Sutherland
anthraquinone-2-carboxylic acid
(1967b)
(ptilometric acid)
79
7-Hydroxy-8-methoxy-6-methyl224-226
Prota et al. (1971, 1972)
1,2-anthraquinone (hallachrome)
(dec)
82
2,5,1O-Trihydroxy-4-methoxy300
van Duijn (1952b)
benzo [#]pyrene-6,12-quinone
(dec)
(arenicochromine)
84
Taondiol
283-284
Gonzalez et al. (1971)
α Subi (sublimation) implies volatilization or resolidification without structural change;
dec (decomposition) implies structural change.