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[ CAS No. 313545-72-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 313545-72-1
Chemical Structure| 313545-72-1
Structure of 313545-72-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 313545-72-1 ]

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Product Details of [ 313545-72-1 ]

CAS No. :313545-72-1 MDL No. :MFCD02684295
Formula : C6H5BClFO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :XOFNMNLYGPKKOV-UHFFFAOYSA-N
M.W : 174.37 Pubchem ID :17750229
Synonyms :

Calculated chemistry of [ 313545-72-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 41.24
TPSA : 40.46 ?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) : -6.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.55
Log Po/w (WLOGP) : 0.58
Log Po/w (MLOGP) : 1.31
Log Po/w (SILICOS-IT) : 0.35
Consensus Log Po/w : 0.76

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.24
Solubility : 1.01 mg/ml ; 0.00582 mol/l
Class : Soluble
Log S (Ali) : -2.01
Solubility : 1.71 mg/ml ; 0.00979 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.18
Solubility : 1.15 mg/ml ; 0.00661 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 313545-72-1 ]

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 [ 313545-72-1 ]

* 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 [ 313545-72-1 ]

[ 313545-72-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 101335-11-9 ]
  • [ 313545-72-1 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; isopropylmagnesium chloride; In tetrahydrofuran; diethyl ether; Trimethyl borate; Intermediate XI A solution of isopropyl magnesium chloride (100 mL, 2.0M in Ethyl Ether) was added to a solution of <strong>[101335-11-9]2-chloro-4-fluoro-1-iodobenzene</strong> (25 g, 97.5 mmol) in 300 mL THF chilled in an ice bath. The solution was then stirred at RT overnight. The solution was chilled in a CO2/acetone bath and trimethyl borate was added (23 mL, 200 mmol). The solution was warmed to RT and stirred for 6 h. The suspension was partitioned between water and ethyl ether (emulsion). The phases were separated and the organic phase concentrated. The residue was treated with 200 mL 2N HCl and stirred overnight. The suspension was then extracted with ethyl ether (2*) and the combined organics washed with brine, dried over MgSO4, filtered and concentrated to give 13.3 g solid. The crude solid was suspended in hexanes, filtered and washed 2* (hexanes) to give 2-chloro-4-fluoro-phenylboronic acid. LC 1: 1.65 min.
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