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[ CAS No. 866607-09-2 ] {[proInfo.proName]}

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Chemical Structure| 866607-09-2
Chemical Structure| 866607-09-2
Structure of 866607-09-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 866607-09-2 ]

CAS No. :866607-09-2 MDL No. :MFCD08706282
Formula : C7H7BF2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :FGQKXEUNYFZVMW-UHFFFAOYSA-N
M.W : 187.94 Pubchem ID :17750069
Synonyms :

Calculated chemistry of [ 866607-09-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 42.86
TPSA : 49.69 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.2 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.75
Log Po/w (WLOGP) : 0.81
Log Po/w (MLOGP) : 0.33
Log Po/w (SILICOS-IT) : -0.3
Consensus Log Po/w : 0.52

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.25
Solubility : 1.05 mg/ml ; 0.00561 mol/l
Class : Soluble
Log S (Ali) : -2.41
Solubility : 0.73 mg/ml ; 0.00388 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.64
Solubility : 4.34 mg/ml ; 0.0231 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.12

Safety of [ 866607-09-2 ]

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 [ 866607-09-2 ]

* 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 [ 866607-09-2 ]

[ 866607-09-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73183-34-3 ]
  • [ 262587-05-3 ]
  • [ 866607-09-2 ]
YieldReaction ConditionsOperation in experiment
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; water; potassium acetate; In 1,4-dioxane; at 100℃; for 17h;Inert atmosphere; [1603j KOAc (26.4 g, 269 mmol), bisQ,inacolato)diboron (30 g, 116 mmol), 3- (difluoromethoxy)bromobenzene (20 g, 90 mmol) and PdC12(dppf) (7.3 g, 9 mmol) were suspended in dry 1,4- dioxane (280 ml) and heated at 100 C under N2 for 17 h. After cooling to room temperature, the mixture was diluted with EtOAc (600 mL) and water (200 mL). The mixture was then filtered via Celite, and washed with EtOAc (200 mL). The organic layer was separated, and the aqueous layer was extracted with EtOAc (200 mL). The combined organic layer was dried over MgSO4 and concentrated. The crude product was used for the next step without further purification.
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