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| Year of first isolation: | 2010 |  | Formula: | C32H50O8 |  | Molecular weight: | 562 |  | Occurence in plants: |  | Silene viridiflora [Caryophyllaceae] »   ![Wikipedia: Silene viridiflora [Caryophyllaceae]](/images/wikipedia.png) 
 |  | Occurence in animals: |  |  |  |   |  |
 | | Canonical SMILES | CC(=O)OC(C)(C)CCC1C(OC(O1)(C)C)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O |  | Isomeric SMILES [ PubChem: search | XML ]
 [ ChemSpider: search ]
 | C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2CC[C@]2([C@]1(CC[C@@H]2[C@]1(C)[C@@H](CCC(C)(C)OC(=O)C)OC(O1)(C)C)O)C)C »  
 |  | IUPAC Name | [2-methyl-4-[(4R,5R)-2,2,5-trimethyl-5-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-1,3-dioxolan-4-yl]butan-2-yl] acetate |  | CAS-RN |  |  | PubChem CID | 12094571 |  | InChiKey [ ChemIDPlus: search ]
 | BFWMUJOITOHIFF-IBVQXDPUSA-N |  | InChI | InChI=1S/C32H50O8/c1-18(33)38-27(2,3)12-11-26-31(8,40-28(4,5)39-26)25-10-14-32(37)20-15-22(34)21-16-23(35)24(36)17-29(21,6)19(20)9-13-30(25,32)7/h15,19,21,23-26,35-37H,9-14,16-17H2,1-8H3/t19-,21-,23+,24-,25-,26+,29+,30+,31+,32+/m0/s1 | 
 
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 | | EI-MS m/z (relative intensity %) |  |  | HR-ESI-MS | 563.35709 [M+H]+, calculated 563.35784 for C32H51O8; 545.34671 [M+H-H2O]+, calculated 545.34728 for C32H49O7 |  | CI-MS (NH3) m/z |  | 
 
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 | | D2O |  | 01 | 37.9 |  | 02 | 69.9 |  | 03 | 69.8 |  | 04 | 33.8 |  | 05 | 52.9 |  | 06 | * |  | 07 | 123.6 |  | 08 | * |  | 09 | 36.5 |  | 10 | 40.7 |  | 11 | 22.5 |  | 12 | 33.2 |  | 13 | 49.4 |  | 14 | 87.7 |  | 15 | 33.0 |  | 16 | 23.6 |  | 17 | 52.1 |  | 18 | 19.4 |  | 19 | 25.7 |  | 20 | 88.5 |  | 21 | 23.6 |  | 22 | 84.7 |  | 23 | 25.6 |  | 24 | 40.2 |  | 25 | 86.7 |  | 25-OAc | 176.1,  24.7 (CH3) |  | 26 | 27.8 |  | 27 | 28.1 |  | C(CH3)2 | 110.5,  28.5 (CH3a),  30.8 (CH3b) | 
 | | D2O |  | 01-Ha | 1.38 (t, 13) |  | 01-He | 1.88 |  | 02-Ha | 3.99 (m, w1/2 = 22) |  | 03-He | 4.07 (m, w1/2 = 8) |  | 04-Ha | 1.75 |  | 04-He | 1.75 |  | 05-H | 2.36 (t) |  | 07-H | 5.97 (d, 2.5) |  | 09-H | 3.11 (m, w1/2 = 22) |  | 11-Ha | 1.73 |  | 11-He | 1.86 |  | 12-Ha | 1.95 |  | 12-He | 1.95 |  | 15-Ha | 1.68a |  | 15-Hb | 1.98a |  | 16-Ha | 2.03b |  | 16-Hb | 1.93b |  | 17-H | 2.28 (t, 9) |  | 18-Me | 0.819 (s) |  | 19-Me | 1.000 (s) |  | 21-Me | 1.240 (s) |  | 22-H | 3.88 (m) |  | 23-Ha | 1.59 |  | 23-Hb | 1.59 |  | 24-Ha | 1.96 |  | 24-Hb | 1.96 |  | 25-OAc | 2.048 (s) (CH3) |  | 26-Me | 1.462 (s) |  | 27-Me | 1.491 (s) |  | C(CH3)2 | 1.407 (s) (CH3a), 1.481 (s) (CH3b) | 
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 | | M.P. | °C ; |  | [α]D20 | ° (c ; MeOH) |  | IR (KBr) ν max (cm-1) |  |  | UV (EtOH) λ max (log ε) | () ; | 
 
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 |  | Permanent link to this datasheet: 20-HYDROXYECDYSONE-20,22-ACETONIDE 25-ACETATE |  |