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[ CAS No. 15115-52-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 15115-52-3
Chemical Structure| 15115-52-3
Structure of 15115-52-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 15115-52-3 ]

CAS No. :15115-52-3 MDL No. :MFCD00234505
Formula : C9H7BrN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :DWPRPWBNLNTEFZ-UHFFFAOYSA-N
M.W : 223.07 Pubchem ID :786811
Synonyms :

Calculated chemistry of [ 15115-52-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 51.26
TPSA : 17.82 ?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) : -5.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.3
Log Po/w (XLOGP3) : 2.58
Log Po/w (WLOGP) : 2.63
Log Po/w (MLOGP) : 2.45
Log Po/w (SILICOS-IT) : 2.21
Consensus Log Po/w : 2.44

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.46
Solubility : 0.0772 mg/ml ; 0.000346 mol/l
Class : Soluble
Log S (Ali) : -2.6
Solubility : 0.557 mg/ml ; 0.0025 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.79
Solubility : 0.0365 mg/ml ; 0.000164 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 15115-52-3 ]

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

Application In Synthesis of [ 15115-52-3 ]

* 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 [ 15115-52-3 ]
  • Downstream synthetic route of [ 15115-52-3 ]

[ 15115-52-3 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 15115-52-3 ]
  • [ 73183-34-3 ]
  • [ 1002334-12-4 ]
YieldReaction ConditionsOperation in experiment
50% With potassium acetate In dimethyl sulfoxide at 20 - 80℃; To a solution of compound 4-bromo-l -phenyl- lH-pyrazo Ie (0.5 g, 2.3 mmol) in DMSO (50 mL) was added KOAc (0.66 g, 6.8 mmol), bis(pinacolato)diboron (0.63 g, 2.5 mmol) and .yen.dCb(dpp{) (0.076g, 0.11 mmol) at room temperature. The reaction mixture was stirred overnight at 8O0C. The result mixture was diluted with EA, washed with brine, dried over Na2SO4, concentrated, purified by chromatography (EA:PE=1: 12) to give l-phenyl-4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)-lH- pyrazole (0.3 g, 50percent) as light yellow solid
Reference: [1] Patent: WO2009/155527, 2009, A2, . Location in patent: Page/Page column 134
  • 2
  • [ 15115-52-3 ]
  • [ 1201643-70-0 ]
Reference: [1] Patent: WO2009/155527, 2009, A2,
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