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[ CAS No. 146328-85-0 ] {[proInfo.proName]}

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Chemical Structure| 146328-85-0
Chemical Structure| 146328-85-0
Structure of 146328-85-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 146328-85-0 ]

CAS No. :146328-85-0 MDL No. :MFCD00143423
Formula : C7H4BrFO2 Boiling Point : -
Linear Structure Formula :- InChI Key :PEXAZYDITWXYNJ-UHFFFAOYSA-N
M.W : 219.01 Pubchem ID :2736315
Synonyms :

Calculated chemistry of [ 146328-85-0 ]      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 : 1.0
Molar Refractivity : 41.06
TPSA : 37.3 ?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) : -5.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.49
Log Po/w (XLOGP3) : 3.13
Log Po/w (WLOGP) : 2.71
Log Po/w (MLOGP) : 2.79
Log Po/w (SILICOS-IT) : 2.32
Consensus Log Po/w : 2.49

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.51
Solubility : 0.0681 mg/ml ; 0.000311 mol/l
Class : Soluble
Log S (Ali) : -3.58
Solubility : 0.0573 mg/ml ; 0.000262 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.269 mg/ml ; 0.00123 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.39

Safety of [ 146328-85-0 ]

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 [ 146328-85-0 ]

* 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 [ 146328-85-0 ]

[ 146328-85-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3095-48-5 ]
  • [ 146328-85-0 ]
  • [ 1529760-76-6 ]
YieldReaction ConditionsOperation in experiment
69% Scheme 6, step A. To a solution of 5-bromo-2-fluorobenzoic acid (3.50 g, 15.9mmol) in CH2Ch (50 mL) at 0 oc are added methyl4-amino-3,5-dimethylbenzoate (2.86g, 15.9 mmol, see preparation 12) and N,N-diisopropylethylamine (8.35 ml, 47.9 mmol).After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50percent solution in ethyl acetate, 20.5 ml, 31.9 mmol) is added via syringe andstirred at ambient temperature. After 36 hours, the solvent is removed under reducedpressure and the residue is diluted with water and extracted with ethyl acetate. Theorganic layers are combined and dried over anhydrous Na2S04, filtered, and concentratedunder reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using 10percent ethyl acetate in hexane to give the title compound as a white solid (4.20g, 69 percent). Mass spectrum (m/z): 380.2 (M+1).
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