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[ CAS No. 289038-22-8 ] {[proInfo.proName]}

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Chemical Structure| 289038-22-8
Chemical Structure| 289038-22-8
Structure of 289038-22-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 289038-22-8 ]

CAS No. :289038-22-8 MDL No. :MFCD00672928
Formula : C7H3BrClFO2 Boiling Point : -
Linear Structure Formula :- InChI Key :GJVIVXZNTOVQRG-UHFFFAOYSA-N
M.W : 253.45 Pubchem ID :2773265
Synonyms :

Calculated chemistry of [ 289038-22-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
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 : 46.07
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) : -5.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.62
Log Po/w (XLOGP3) : 2.87
Log Po/w (WLOGP) : 3.36
Log Po/w (MLOGP) : 3.36
Log Po/w (SILICOS-IT) : 2.98
Consensus Log Po/w : 2.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.52
Solubility : 0.0759 mg/ml ; 0.0003 mol/l
Class : Soluble
Log S (Ali) : -3.31
Solubility : 0.123 mg/ml ; 0.000487 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.52
Solubility : 0.076 mg/ml ; 0.0003 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.68

Safety of [ 289038-22-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 289038-22-8 ]

* 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 [ 289038-22-8 ]

[ 289038-22-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 951884-02-9 ]
  • [ 289038-22-8 ]
YieldReaction ConditionsOperation in experiment
5-Bromo-4-chloro-2-fluoro-benzoic acid methyl ester (14.0 g, 52.4 mmol) was stirred vigorously in a mixture of THF (250 ml) and 1 N NaOH (200 ml) for 16 hrs. The mixture was acidified to pH 3 with 6N HCI, concentrated partially to remove THF and then extracted with ethyl acetate. The organic phase was washed with water and brine and was dried over Na2SO4. The filtrate was concentrated to yield 5-bromo- 4-chloro-2-fluoro-benzoic acid (13.3 g).
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