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[ CAS No. 99725-13-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 99725-13-0
Chemical Structure| 99725-13-0
Structure of 99725-13-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 99725-13-0 ]

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Product Details of [ 99725-13-0 ]

CAS No. :99725-13-0 MDL No. :MFCD00143425
Formula : C7H6BrFO Boiling Point : No data available
Linear Structure Formula :- InChI Key :UOSBHJFKMGLWGX-UHFFFAOYSA-N
M.W : 205.02 Pubchem ID :2773352
Synonyms :

Calculated chemistry of [ 99725-13-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.23
TPSA : 20.23 ?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) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.07
Log Po/w (XLOGP3) : 1.62
Log Po/w (WLOGP) : 2.35
Log Po/w (MLOGP) : 2.72
Log Po/w (SILICOS-IT) : 2.77
Consensus Log Po/w : 2.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.51
Solubility : 0.634 mg/ml ; 0.00309 mol/l
Class : Soluble
Log S (Ali) : -1.66
Solubility : 4.52 mg/ml ; 0.022 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.36
Solubility : 0.0887 mg/ml ; 0.000433 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.35

Safety of [ 99725-13-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 99725-13-0 ]

* 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 [ 99725-13-0 ]

[ 99725-13-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 99725-13-0 ]
  • [ 481681-02-1 ]
YieldReaction ConditionsOperation in experiment
To a solution of 5-bromo-2-fluoro-benzylalcohol [(L.] Oeq. ) from Step 1 in THF (0. [1M)] at-78C was added dropwise n-BuLi (2.2eq.). The mixture was stirred at-78C for 15min then [TRI-ISOPROPYLBORONATE] (2.2eq.) was added. The final mixture was warm slowly to rt, stirred for lh and quenched with HCl [(1M).] After stirring for lh, the mixture was extracted with EtOAc (2x). The combined organic extracts were washed with water, brine, dried over [NA2SO4,] filtered and concentrated. Stirring in Hex: EtOAc: H20 (90: 9: 1) for 12h afforded the title compound which was isolated by filtration as a white solid.
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