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[ CAS No. 106312-36-1 ] {[proInfo.proName]}

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Chemical Structure| 106312-36-1
Chemical Structure| 106312-36-1
Structure of 106312-36-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 106312-36-1 ]

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Product Citations

Product Details of [ 106312-36-1 ]

CAS No. :106312-36-1 MDL No. :MFCD01091011
Formula : C9H7F3O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BVPVUMRIGHMFNV-UHFFFAOYSA-N
M.W : 204.15 Pubchem ID :2778286
Synonyms :

Calculated chemistry of [ 106312-36-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.32
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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 2.24
Log Po/w (WLOGP) : 3.68
Log Po/w (MLOGP) : 2.16
Log Po/w (SILICOS-IT) : 3.02
Consensus Log Po/w : 2.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.64
Solubility : 0.472 mg/ml ; 0.00231 mol/l
Class : Soluble
Log S (Ali) : -2.43
Solubility : 0.762 mg/ml ; 0.00373 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.37
Solubility : 0.0879 mg/ml ; 0.000431 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.5

Safety of [ 106312-36-1 ]

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

Application In Synthesis of [ 106312-36-1 ]

* 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.

  • Upstream synthesis route of [ 106312-36-1 ]

[ 106312-36-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 106312-36-1 ]
  • [ 1243395-68-7 ]
YieldReaction ConditionsOperation in experiment
91%
Stage #1: With boron tribromide In dichloromethane at -78 - 20℃;
Stage #2: With water In dichloromethane
A solution of boron tribromide (1.39 ml, 14.7 mmol) in 5 ml of DCM was added dropwise to a solution of 4-methoxy-2-trifluoromethylbenzaldehyde (2.Og, 9.8 mmol) in 20 ml of DCM at -78 0C. The reaction mixture was stirred at room temperature for 15 h. Then the reaction mixture was quenched with ice water and extracted with DCM. The combined organic extracts were washed with bicarbonate solution, water, and brine, and dried over sodium sulfate and concentrated under reduced pressure. The crude material was purified by silica column using a hexane-EtOAc system to give 4-hydroxy-2- trifluoromethylbenzaldehyde as a brownish liquid in 91percent yield. 1H-NMR (400 MHz, DMSO-d6) δ 10.035 (s, IH), 7.984-7.963 (d, IH, J= 8.4), 7.193-7.158 (m, 2H) ppm.
86% With boron tribromide In dichloromethane at -78 - 20℃; for 5 h; Inert atmosphere To a mixture of A-16 (2 g, 9.80 mmol) in dichloromethane (30 mL) was added BBr3 (4M in DCM, 2 mL) at ?78° C. The reaction was stirred for 5 h at room temperature. Water was added, the mixture was extracted with dichloromethane thrice. The combined extracts were washed with H2O, brine and dried over Na2SO4. Concentration and chromatograph on silica gel (2:1 PE/EtOAc) gave 1.6 g (86percent) of B-16 as a white solid.
Reference: [1] Patent: WO2010/127208, 2010, A1, . Location in patent: Page/Page column 53
[2] Patent: US2014/256657, 2014, A1, . Location in patent: Paragraph 0417
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Technical Information

? Acidity of Phenols ? Alkyl Halide Occurrence ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs 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 ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nomenclature of Ethers ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? 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 ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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