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[ CAS No. 555-66-8 ] {[proInfo.proName]}

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Chemical Structure| 555-66-8
Chemical Structure| 555-66-8
Structure of 555-66-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 555-66-8 ]

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Product Details of [ 555-66-8 ]

CAS No. :555-66-8 MDL No. :MFCD01736094
Formula : C17H24O3 Boiling Point : -
Linear Structure Formula :- InChI Key :OQWKEEOHDMUXEO-BQYQJAHWSA-N
M.W : 276.37 Pubchem ID :5281794
Synonyms :
[6]-Shogaol;6-Shogaol
Chemical Name :1-(4-Hydroxy-3-methoxyphenyl)dec-4-en-3-one

Calculated chemistry of [ 555-66-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.47
Num. rotatable bonds : 9
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 82.91
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.28
Log Po/w (XLOGP3) : 3.99
Log Po/w (WLOGP) : 4.04
Log Po/w (MLOGP) : 2.9
Log Po/w (SILICOS-IT) : 4.61
Consensus Log Po/w : 3.76

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.7
Solubility : 0.0558 mg/ml ; 0.000202 mol/l
Class : Soluble
Log S (Ali) : -4.67
Solubility : 0.00593 mg/ml ; 0.0000214 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.8
Solubility : 0.00435 mg/ml ; 0.0000157 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.51

Safety of [ 555-66-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 555-66-8 ]

* 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.

  • Upstream synthesis route of [ 555-66-8 ]

[ 555-66-8 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 555-66-8 ]
  • [ 27113-22-0 ]
YieldReaction ConditionsOperation in experiment
98% With palladium 10% on activated carbon; hydrogen In tetrahydrofuran at 20℃; Synthesis of 1-(4'-hydroxy-3'-methoxyphenyl)-decan-3-one (M11)
A solution of [6]-shogaol (276 mg, 1.0 mmol) in THF (2 mL) at rt was treated with 10percent Pd/C (30 mg, 10percent w/w) under H2.
The mixture was stirred at rt overnight and filtered.
The filtrate was concentrated under reduced pressure.
The residue was loaded to preparative TLC (hexane/EtOAc=8:1) to give the title compound M11 as a yellow oil (272 mg, yield 98percent); 1H NMR (600 MHz, CDCl3) δ 6.69 (1H, d, J=1.6 Hz, H-2'), 6.82 (1H, d, J=8.0 Hz, H-5'), 6.66 (1H, dd, J=8.0, 1.7 Hz, H-6'), 2.69 (2H, t, J=7.4 Hz, H-1), 2.82 (2H, t, J 7.4 Hz, H-2), 2.37 (1H, t, J=7.4 Hz, H-4), 1.54 (2H, m, H-5), 1.30-1.24 (8H, m, ranged from H-6 to H-9), 0.87 (3H, t, J=6.8 Hz, H-10), and 3.87 (3H, s, OMe-3'); positive APCIMS, m/z 279 [M+H]+.
Reference: [1] Patent: US9272994, 2016, B1, . Location in patent: Page/Page column 51
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Technical Information

? Acidity of Phenols ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Nomenclature of Ethers ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Ethers ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Ethers ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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