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[ CAS No. 74457-86-6 ] {[proInfo.proName]}

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Chemical Structure| 74457-86-6
Chemical Structure| 74457-86-6
Structure of 74457-86-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 74457-86-6 ]

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Product Citations

Product Details of [ 74457-86-6 ]

CAS No. :74457-86-6 MDL No. :MFCD00042290
Formula : C9H9FO2 Boiling Point : -
Linear Structure Formula :- InChI Key :PIRRWUMTIBFCCW-UHFFFAOYSA-N
M.W : 168.17 Pubchem ID :592821
Synonyms :

Calculated chemistry of [ 74457-86-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.09
TPSA : 26.3 ?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) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.87
Log Po/w (XLOGP3) : 1.99
Log Po/w (WLOGP) : 2.46
Log Po/w (MLOGP) : 1.86
Log Po/w (SILICOS-IT) : 2.58
Consensus Log Po/w : 2.15

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.37
Solubility : 0.71 mg/ml ; 0.00422 mol/l
Class : Soluble
Log S (Ali) : -2.17
Solubility : 1.14 mg/ml ; 0.00678 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.13
Solubility : 0.124 mg/ml ; 0.000736 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.36

Safety of [ 74457-86-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 74457-86-6 ]

* 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 [ 74457-86-6 ]

[ 74457-86-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 74457-86-6 ]
  • [ 157014-35-2 ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 106 2-Bromo-2'-fluoro-4'-methoxyacetophenone (VI) Following the general procedure of EXAMPLE 100 and making non-critical variations but starting with 2'fluoro-4'-methoxyacetophenone (Aldrich Chemical Co.), the title compound is obtained, mp 67-69; NMR (CDCl3, TMS) 7.95, 6.79, 6.64, 4.48δ; HRMS (EI, m/z) calculated for C9 H8 BrFO2 M+ found=246 and 248.
  • 2
  • [ 10102-94-0 ]
  • [ 74457-86-6 ]
  • (E)-3-(5-bromo-1-methyl-1H-indol-3-yl)-1-(2-fluoro-4-methoxyphenyl)prop-2-en-1-one [ No CAS ]
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Technical Information

? Acidity of Phenols ? Alkyl Halide Occurrence ? 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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