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[ CAS No. 39503-52-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 39503-52-1
Chemical Structure| 39503-52-1
Structure of 39503-52-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 39503-52-1 ]

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Product Citations

Product Details of [ 39503-52-1 ]

CAS No. :39503-52-1 MDL No. :MFCD03426751
Formula : C9H9BrO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WLCVGKZBHDBQJN-UHFFFAOYSA-N
M.W : 261.07 Pubchem ID :1051517
Synonyms :

Calculated chemistry of [ 39503-52-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 53.94
TPSA : 55.76 ?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) : -6.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.62
Log Po/w (XLOGP3) : 2.63
Log Po/w (WLOGP) : 1.95
Log Po/w (MLOGP) : 1.77
Log Po/w (SILICOS-IT) : 1.93
Consensus Log Po/w : 2.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.23
Solubility : 0.152 mg/ml ; 0.000583 mol/l
Class : Soluble
Log S (Ali) : -3.45
Solubility : 0.0924 mg/ml ; 0.000354 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.88
Solubility : 0.343 mg/ml ; 0.00131 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.84

Safety of [ 39503-52-1 ]

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

Application In Synthesis of [ 39503-52-1 ]

* 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 [ 39503-52-1 ]

[ 39503-52-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1398331-98-0 ]
  • [ 39503-52-1 ]
  • C19H20O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate; In 1,4-dioxane; at 100℃; for 5.0h;Inert atmosphere; Taking compound 3 d (131 mg, 0.5 mmol), compound 4 (137 mg, 0.5 mmol), PdCl2(Dppf) DCM (20 mg, 0 . 025 mmol) and potassium carbonate (207 mg, 1.5 mmol) is placed in a thick-wall pressure reaction tube, add 1, 4 - dioxane (2 ml), nitrogen advocated for 5 min, for 100 C heating 5 h. TLC monitoring display after the reaction. Placing to room temperature, filtered through diatomaceous earth, to ethyl acetate (10 ml) washing, turns on lathe does the filtrate, the residue by silica gel column chromatography (petroleum ether: ethyl acetate=15:1) purification to obtain compound 5 d (voscosity, 118 mg, yield 72%).
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Technical Information

? Acidity of Phenols ? Acyl Group Substitution ? Alkyl Halide Occurrence ? Appel Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bouveault-Blanc Reduction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Complex Metal Hydride Reductions ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Electrophilic Substitution of the Phenol Aromatic Ring ? Ester Cleavage ? Etherification Reaction of Phenolic Hydroxyl Group ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Halogenation of Phenols ? Hiyama Cross-Coupling Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Martin's Sulfurane Dehydrating Reagent ? Mitsunobu Reaction ? Moffatt Oxidation ? Nomenclature of Ethers ? Oxidation of Alcohols by DMSO ? Oxidation of Phenols ? Pechmann Coumarin Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Ethers ? Reactions of Alcohols ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Dihalides ? Reactions of Ethers ? Reactions with Organometallic Reagents ? Reimer-Tiemann Reaction ? Ritter Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Stille Coupling ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Vilsmeier-Haack Reaction
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