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CAS No. : | 103536-97-6 | MDL No. : | MFCD30342469 |
Formula : | C12H18O4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | VPRMGOPLYBDBLB-DDHJBXDOSA-N |
M.W : | 226.27 g/mol | Pubchem ID : | 90017848 |
Synonyms : |
|
Num. heavy atoms : | 16 |
Num. arom. heavy atoms : | 0 |
Fraction Csp3 : | 0.67 |
Num. rotatable bonds : | 6 |
Num. H-bond acceptors : | 4.0 |
Num. H-bond donors : | 0.0 |
Molar Refractivity : | 58.96 |
TPSA : | 36.92 Ų |
GI absorption : | High |
BBB permeant : | Yes |
P-gp substrate : | No |
CYP1A2 inhibitor : | No |
CYP2C19 inhibitor : | No |
CYP2C9 inhibitor : | No |
CYP2D6 inhibitor : | No |
CYP3A4 inhibitor : | No |
Log Kp (skin permeation) : | -7.15 cm/s |
Log Po/w (iLOGP) : | 2.72 |
Log Po/w (XLOGP3) : | 0.74 |
Log Po/w (WLOGP) : | 0.93 |
Log Po/w (MLOGP) : | 0.11 |
Log Po/w (SILICOS-IT) : | 1.84 |
Consensus Log Po/w : | 1.27 |
Lipinski : | 0.0 |
Ghose : | None |
Veber : | 0.0 |
Egan : | 0.0 |
Muegge : | 0.0 |
Bioavailability Score : | 0.55 |
Log S (ESOL) : | -1.31 |
Solubility : | 11.0 mg/ml ; 0.0486 mol/l |
Class : | Very soluble |
Log S (Ali) : | -1.09 |
Solubility : | 18.2 mg/ml ; 0.0805 mol/l |
Class : | Very soluble |
Log S (SILICOS-IT) : | -1.29 |
Solubility : | 11.6 mg/ml ; 0.0514 mol/l |
Class : | Soluble |
PAINS : | 0.0 alert |
Brenk : | 1.0 alert |
Leadlikeness : | 1.0 |
Synthetic accessibility : | 4.09 |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
94% | With potassium tert-butylate; In N,N-dimethyl-formamide; at 0 - 20℃;Inert atmosphere; | Dialylisomannide, (3R,3aR,6R,6aR)-3,6-bis(allyloxy)hexahydrofuro[3,2-b]furan, was synthesized as follows: A dry, 2-neck, 100 mL boiling flask was charged with 2.00 g of isomannide (13.7rnmol), 3 .. 38 g of potassium t-butoxide (30. 1 mmol) and 25 ml ofdimethylformamide. A rubber septum was placed over one of the necks, whilean argon llne was outfitted onto the other. The heterogeneous mixture waspurged with argon, and concomitantly cooled to about 0 degrees Celsius in abrine/ice bath. While vigorously stirring, 2.38 mL (27.4 mmol) of ally bromidewas injected through the septum over 15 minutes. Once complete additionhad occurred, the ice bath was removed, allowing the reaction mixture towarm to room temperature overnight. After this time, a light yellow solutionwith profuse white precipitate was observed. The solution was transferred toa 250 ml round bottomed flask, and diluted with 100 mL of methylenecl1loride and 1. 00 ml of water. The water addition quickly dissolved the solidsand resultant biphasic mixture was stirred vigorously. The bottorn organicphase was removed and diluted witt1 100 rnL more of water. After stirring, theorganic phase was again removed, dried with anhydrous magnesium sulfateand concentrated in vacuo, furnishing a loose, light yellow oil, 2.92 g {94% oftheoretical yield). Thin layer chromatography (5:1 hexanes/ethyl acetate)indicated only one spot (rt = 0.4). 1 H NMR (CDCI3, 400 MHz) o (ppm) 5.90-5.88 (m, 2H), 5.29 (d, J = 4.2 Hz. 1H), 5.27 (d. J = 6.8 Hz, 2H), 5.25 (d, J =3.8 Hz. 1H), 5.16 (d, J = 7.8 Hz, 2H),4.50 (d, J = 3.0 Hz, 2H), 4.13 (d, J = 3.3Hz. 1 H), 4.11 (d, J = 3.8 Hz, 1 H), 4.04-4.00 (rn. 5H), 3.68 (s, 1 H). 13C NMR{CDCI3, 125 MHz) o (ppm) 134.74, 117.95, 80.63, 79.90, 71.91, 71.26. |
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