+++ Свойства аромадендрина

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Здравствуйте!
Помогите, пожалуйста, кто может с поиском свойств аромадендрина.
С15Н12О6
Заранее большое спасибо!

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Experimental Properties: Optical and Scattering Spectra Thermal
Top Optical and Scattering Properties Value Condition Note
Optical Rotatory Power +105.2 ° Conc: 0.03 g/100mL; Solv: methanol (67-56-1); Wavlen: 365 nm; Temp: 25 °C (10) IC
Optical Rotatory Power +53 ° Conc: 0.1 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 20 °C (4) CAS
Optical Rotatory Power +51.7 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 20 °C (18) CAS
Optical Rotatory Power +51.5 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 25 °C (17) CAS
Optical Rotatory Power +47 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 22 °C (23) CAS
Optical Rotatory Power +46.3 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 20 °C (18) CAS
Optical Rotatory Power +45 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 20 °C (22) CAS
Optical Rotatory Power +38.6 ° Conc: 0.145 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 22 °C (5) CAS
Optical Rotatory Power +34.0 ° Conc: 0.5 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 25 °C (3) CAS
Optical Rotatory Power +29 ° Solv: acetone (67-64-1), water (7732-18-5); Wavlen: 589.3 nm; Temp: 21 °C (19) CAS
Optical Rotatory Power +27 ° Solv: acetone (67-64-1); Wavlen: 589.3 nm; Temp: 22 °C (23) CAS
Optical Rotatory Power +26.5 ° Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 25 °C (17) CAS
Optical Rotatory Power +25.9 ° Conc: 0.98 g/100mL; Solv: methanol (67-56-1); Wavlen: 435 nm; Temp: 25 °C (10) IC
Optical Rotatory Power +22.8 ° Conc: 1.32 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 23 °C (2) CAS
Optical Rotatory Power +22.1 ° Conc: 0.60 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm (27) CAS
Optical Rotatory Power +11.5 ° Conc: 0.98 g/100mL; Solv: methanol (67-56-1); Wavlen: 546 nm; Temp: 25 °C (10) IC
Optical Rotatory Power +10.7 ° Conc: 0.35 g/100mL; Solv: methanol (67-56-1); Wavlen: 589.3 nm; Temp: 24 °C (6) CAS
Optical Rotatory Power +9.5 ° Conc: 0.98 g/100mL; Solv: methanol (67-56-1); Wavlen: 589 nm; Temp: 25 °C (10) IC
Optical Rotatory Power See full text (20) CAS
Top Spectra Properties Value Condition Note
Carbon-13 NMR Spectrum See full text (2) CAS
Carbon-13 NMR Spectrum See full text (3) CAS
Carbon-13 NMR Spectrum See full text (4) CAS
Carbon-13 NMR Spectrum See full text (5) CAS
Carbon-13 NMR Spectrum See full text (6) CAS
Carbon-13 NMR Spectrum See full text (7) CAS
Carbon-13 NMR Spectrum See full text (8) CAS
IR Absorption Spectrum See full text (2) CAS
IR Absorption Spectrum See full text (3) CAS
IR Absorption Spectrum See full text (9) CAS
IR Absorption Spectrum See full text (5) CAS
IR Absorption Spectrum See full text (10) IC
Mass Spectrum See spectrum (11) WSS
Mass Spectrum See full text (5) CAS
Mass Spectrum See full text (2) CAS
Mass Spectrum See full text (4) CAS
Mass Spectrum See full text (8) CAS
Mass Spectrum See full text (7) CAS
Mass Spectrum See full text (6) CAS
Mass Spectrum See full text (9) CAS
Mass Spectrum See full text (10) IC
Mass Spectrum See full text (12) CAS
Mass Spectrum See full text (13) CAS
Mass Spectrum See full text (14) CAS
Mass Spectrum See full text (15) CAS
Mass Spectrum See full text (16) CAS
NMR Spectrum See full text (26) CAS
NMR Spectrum See full text (15) CAS
Proton NMR Spectrum See full text (5) CAS
Proton NMR Spectrum See full text (2) CAS
Proton NMR Spectrum See full text (3) CAS
Proton NMR Spectrum See full text (4) CAS
Proton NMR Spectrum See full text (6) CAS
Proton NMR Spectrum See full text (7) CAS
Proton NMR Spectrum See full text (8) CAS
Proton NMR Spectrum See full text (14) CAS
Proton NMR Spectrum See full text (10) IC
UV and Visible Absorption Spectrum See full text (3) CAS
UV and Visible Absorption Spectrum See full text (5) CAS
UV and Visible Absorption Spectrum See full text (14) CAS
UV and Visible Absorption Spectrum See full text (16) CAS
UV and Visible Absorption Spectrum See full text (28) CAS
UV and Visible Absorption Spectrum See full text (8) CAS
UV and Visible Spectrum See full text (7) CAS
UV and Visible Spectrum See full text (6) CAS
Top Thermal Properties Value Condition Note
Boiling Point 139-140 °C (1) CAS
Melting Point 247.0-248.5 °C (17) CAS
Melting Point 247-248 °C (5) CAS
Melting Point 244-245 °C (18) CAS
Melting Point 242-243 °C Solv: water (7732-18-5) (18) CAS
Melting Point 241-242 °C (19) CAS
Melting Point 238-240 °C (20) CAS
Melting Point 238-240 °C (17) CAS
Melting Point 238-240 °C (decomp) (21) CAS
Melting Point 237-239 °C (22) CAS
Melting Point 237.0-238.5 °C (23) CAS
Melting Point 237 °C Solv: chloroform (67-66-3); ethyl acetate (141-78-6) (6) CAS
Melting Point 235-237 °C (4) CAS
Melting Point 228-230 °C (3) CAS
Melting Point 227 °C (24) CAS
Melting Point 224-225 °C (decomp) (25) CAS
Melting Point 220-222 °C Solv: methanol (67-56-1) (7) CAS
Melting Point 206-210 °C Solv: methanol (67-56-1) (10) IC
Melting Point 54-59 °C (1) CAS

(1) Radcliffe, C. B.; Journal of the Chemical Society 1938, P1200-3 CAPLUS
(2) Lee, Eun Ha; Archives of Pharmacal Research 2003, V26(12), P1018-1023 CAPLUS
(3) Zhang, XinFeng; Archives of Pharmacal Research 2006, V29(12), P1102-1108 CAPLUS
(4) Han, Xiang Hua; Archives of Pharmacal Research 2007, V30(1), P13-17 CAPLUS
(5) Jeon, Seong Ho; Archives of Pharmacal Research 2008, V31(8), P978-982 CAPLUS
(6) Fukai, Toshio; Journal of Natural Products 2003, V66(8), P1118-1120 CAPLUS
(7) Backheet, Enaam Y.; Bulletin of Pharmaceutical Sciences, Assiut University 2003, V26(1), P55-66 CAPLUS
(8) Kwak, Jong Hwan; Archives of Pharmacal Research 2009, V32(12), P1681-1687 CAPLUS
(9) Lee, Young Jae; Archives of Pharmacal Research 2009, V32(2), P195-200 CAPLUS
(10) Takahashi, Hiroshi; Chemical & Pharmaceutical Bulletin 1988, V36(5), P1877-81 CAPLUS
(11) WSS: Spectral data were obtained from Wiley Subscription Services, Inc. (US)
(12) Marles, M. A. Susan; Phytochemistry (Elsevier) 2003, V62(5), P663-672 CAPLUS
(13) Dixon, David P.; Journal of Biological Chemistry 2010, V285(47), P36322-36329 CAPLUS
(14) Welford, Richard W. D.; Organic & Biomolecular Chemistry 2005, V3(17), P3117-3126 CAPLUS
(15) Exarchou, Vassiliki; Analytical Chemistry 2003, V75(22), P6288-6294 CAPLUS
(16) Sanz, Miriam; Journal of Agricultural and Food Chemistry 2010, V58(8), P4907-4914 CAPLUS
(17) Hillis, W. E.; Australian Journal of Scientific Research, Series B: Biological Sciences 1952, VA5, P379-86 CAPLUS
(18) Hillis, W. E.; Australian Journal of Chemistry 1963, V16, P147-59 CAPLUS
(19) Laidlaw, R. A.; Chemistry & Industry (London, United Kingdom) 1958, P1325-6 CAPLUS
(20) Arciniegas, Amira; Heterocycles 2009, V78(5), P1253-1263 CAPLUS
(21) FR 1578715 1969 CAPLUS
(22) Gripenberg, Jarl; Acta Chemica Scandinavica 1952, V6, P1152-6 CAPLUS
(23) Erdtman, Holger; Chemische Berichte 1956, V89, P341-3 CAPLUS
(24) Hasegawa, Masao; Shigen Kagaku Kenkyusho Iho 1950, VNo. 17-18, P57-60 CAPLUS
(25) Uoda, Hidetaka; Nippon Nogei Kagaku Kaishi 1943, V19, P467-77 CAPLUS
(26) Moreira, Francisco de Paula Madeira; Quimica Nova 2003, V26(3), P309-311 CAPLUS
(27) Chin, Young-Won; Journal of Agricultural and Food Chemistry 2008, V56(17), P7759-7764 CAPLUS
(28) Regos, Ionela; Journal of Chromatography, A 2010, V1217(40), P6169-6177 CAPLUS

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