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. Author manuscript; available in PMC: 2024 Jan 17.
Published in final edited form as: J Med Chem. 1996 Jun 7;39(12):2293–2301. doi: 10.1021/jm950923i

Table 2.

Physical Characterization of Flavone, Flavanol, and Flavanone Derivatives

compd no. mp (°C) MS formula anal.
2 201 313 (CI) C18H16O5·0.75H2O C,H
3a 111–114 355 (FAB) C21H22O5 C,H
3b 100–101 337 (CI) C19H18O5 C,H
4 90–93 397 (CI) C24H28O5 C,H
6 153–156 373 (CI) C20H20O7 C,H
7 122–123 415 (FAB) C23H26O7 C,H
8 115–116 443 (CI) C25H30O7 C,H
10 oil 293 (CI) C18H12O4 C,H
11b 121 256 (EI) C15H9O2Cl·0.25EtOH C,H
11c 170–172 257 (CI) C15H9O2Cl·O.1H2O C,H
11d 184–186 290 (EI) C15H8O2Cl2 a
15 160–163 297 (CI) C18H16O4·0.25H2O C,H
16 135–138 294 (EI) C18H14O4 a,b
19 175–178 319 (CI) C20H14O4·0.25H2O C,H
20 148–151 333 (CI) C21H16O4 C,H
21 132 347 (CI) C22H18O4 C,H
22 162–165 344 (EI) C22H16O4·0.5H2O C,H
23 162–165 358 (EI) C23H18O4 C,H
24 150–154 320 (CI) C19H14NO4 C,H
a

High-resolution mass in FAB+ mode m/z determined to be within acceptable limits. 11d: calcd, 289.9901; found, 289.9893. 16: calcd, 294.0892; found, 294.0889.

b

C: calcd, 73.46; found, 74.30. H: calcd, 4.80; found, 5.27.