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    [ CAS No. 1201-91-8 ] {[proInfo.proName]}

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    Cat. No.: {[proInfo.prAm]}
    Chemical Structure| 1201-91-8
    Chemical Structure| 1201-91-8
    Structure of 1201-91-8 * Storage: {[proInfo.prStorage]}

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    Product Details of [ 1201-91-8 ]

    CAS No. :1201-91-8 MDL No. :MFCD00963547
    Formula : C10H13NO2 Boiling Point : No data available
    Linear Structure Formula :- InChI Key :JOCUIVLSLBBESN-UHFFFAOYSA-N
    M.W : 179.22 Pubchem ID :3614316
    Synonyms :

    Calculated chemistry of [ 1201-91-8 ]      Expand+

    Physicochemical Properties

    Num. heavy atoms : 13
    Num. arom. heavy atoms : 6
    Fraction Csp3 : 0.3
    Num. rotatable bonds : 4
    Num. H-bond acceptors : 2.0
    Num. H-bond donors : 1.0
    Molar Refractivity : 52.01
    TPSA : 40.54 ?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) : -6.59 cm/s

    Lipophilicity

    Log Po/w (iLOGP) : 1.65
    Log Po/w (XLOGP3) : 1.13
    Log Po/w (WLOGP) : 0.93
    Log Po/w (MLOGP) : 0.86
    Log Po/w (SILICOS-IT) : 1.3
    Consensus Log Po/w : 1.17

    Druglikeness

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

    Water Solubility

    Log S (ESOL) : -1.74
    Solubility : 3.26 mg/ml ; 0.0182 mol/l
    Class : Very soluble
    Log S (Ali) : -1.58
    Solubility : 4.77 mg/ml ; 0.0266 mol/l
    Class : Very soluble
    Log S (SILICOS-IT) : -2.3
    Solubility : 0.894 mg/ml ; 0.00499 mol/l
    Class : Soluble

    Medicinal Chemistry

    PAINS : 0.0 alert
    Brenk : 1.0 alert
    Leadlikeness : 1.0
    Synthetic accessibility : 1.04

    Safety of [ 1201-91-8 ]

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

    ? Appel Reaction ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? Mannich Reaction ? Martin's Sulfurane Dehydrating Reagent ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mitsunobu Reaction ? Moffatt Oxidation ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Alcohols by DMSO ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Alcohols ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stetter Reaction ? Stobbe Condensation ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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    ; ;