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[ CAS No. 1080-12-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1080-12-2
Chemical Structure| 1080-12-2
Structure of 1080-12-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1080-12-2 ]

Related Doc. of [ 1080-12-2 ]

Alternatived Products of [ 1080-12-2 ]
Product Citations

Product Details of [ 1080-12-2 ]

CAS No. :1080-12-2 MDL No. :MFCD00012210
Formula : C11H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :AFWKBSMFXWNGRE-ONEGZZNKSA-N
M.W : 192.21 Pubchem ID :5354238
Synonyms :
Chemical Name :4-(4-Hydroxy-3-methoxyphenyl)but-3-en-2-one

Calculated chemistry of [ 1080-12-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.18
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 54.86
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 1.73
Log Po/w (WLOGP) : 1.89
Log Po/w (MLOGP) : 1.33
Log Po/w (SILICOS-IT) : 2.23
Consensus Log Po/w : 1.86

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.24
Solubility : 1.1 mg/ml ; 0.00574 mol/l
Class : Soluble
Log S (Ali) : -2.32
Solubility : 0.912 mg/ml ; 0.00475 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.38
Solubility : 0.803 mg/ml ; 0.00418 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 1080-12-2 ]

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:

Application In Synthesis of [ 1080-12-2 ]

* 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.

  • Downstream synthetic route of [ 1080-12-2 ]

[ 1080-12-2 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 110-86-1 ]
  • [ 1076-38-6 ]
  • [ 1080-12-2 ]
  • [ 84245-27-2 ]
  • 2
  • [ 54-85-3 ]
  • [ 1080-12-2 ]
  • [ 70988-28-2 ]
  • 3
  • [ 50-00-0 ]
  • [ 1080-12-2 ]
  • [ 6091-44-7 ]
  • [ 55882-97-8 ]
  • 4
  • [ 4438-85-1 ]
  • [ 1080-12-2 ]
  • [ 84245-27-2 ]
  • 5
  • [ 623-11-0 ]
  • [ 1080-12-2 ]
  • [ 121-33-5 ]
  • 6
  • [ 1080-12-2 ]
  • [ 122-48-5 ]
YieldReaction ConditionsOperation in experiment
94% With nickel boride; hydrogen; In methanol; at 25℃; for 1.5h; General procedure: Sodium tetrahydridoborate, 0.46 g (12.1 mmol), was added in portions with stirring to a solution of 1.10 g (4.63 mmol) of NiCl2·6H2O in 20 mL of methanol, cooled to 0 C. The resulting suspension was stirred for 15 min at 0 C and refluxed for 20 min under argon. The mixture was then cooled to room temperature, 9.25 mmol of ketone 1a-1g was added, and the miixture was stirred in a hydrogen atmosphere. When the green color of the reaction mixture disappeared, hydrogen supply was turned off, and the mixture was filtered. The precipitate of nickel boride was additionally washed with a small amount of methanol, and the filtrate was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (20 mL), the solution was washed with a saturated aqueous solution of ammonium chloride (20 mL), the organic phase was separated, and the aqueous phase was extracted with ethyl acetate (10 mL). The combined organic phases were washed with saturated solutions of NaHCO3 and NaCl (10 mL each), dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by crystallization from appropriate solvent mixture or by column chromatography.
  • 7
  • [ 1080-12-2 ]
  • 3-hydroxy-1-(4-hydroxy-3-methoxy-phenyl)-butane-1,3-disulfonic acid [ No CAS ]
  • 8
  • [ 1080-12-2 ]
  • [ 104-88-1 ]
  • 1<i>t</i>(?)-(4-chloro-phenyl)-5<i>t</i>(?)-(4-hydroxy-3-methoxy-phenyl)-penta-1,4-dien-3-one [ No CAS ]
  • 10
  • [ 1080-12-2 ]
  • [ 599-91-7 ]
  • [ 943598-89-8 ]
  • 11
  • [ 1080-12-2 ]
  • [ 100-63-0 ]
  • [ 109567-14-8 ]
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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
Historical Records

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