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[ CAS No. 1416440-62-4 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1416440-62-4
Chemical Structure| 1416440-62-4
Chemical Structure| 1416440-62-4
Structure of 1416440-62-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1416440-62-4 ]

CAS No. :1416440-62-4 MDL No. :MFCD22690572
Formula : C9H5BrClN Boiling Point : -
Linear Structure Formula :- InChI Key :DNPKBKRTVUSVRU-UHFFFAOYSA-N
M.W : 242.50 Pubchem ID :71742993
Synonyms :

Calculated chemistry of [ 1416440-62-4 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.45
TPSA : 12.89 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.38
Log Po/w (XLOGP3) : 3.51
Log Po/w (WLOGP) : 3.65
Log Po/w (MLOGP) : 3.12
Log Po/w (SILICOS-IT) : 3.76
Consensus Log Po/w : 3.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.17
Solubility : 0.0163 mg/ml ; 0.0000674 mol/l
Class : Moderately soluble
Log S (Ali) : -3.46
Solubility : 0.0833 mg/ml ; 0.000343 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.17
Solubility : 0.00162 mg/ml ; 0.00000668 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.5

Safety of [ 1416440-62-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1416440-62-4 ]

* 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 [ 1416440-62-4 ]

[ 1416440-62-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 540-80-7 ]
  • [ 116632-57-6 ]
  • 3-bromo-5-chloroquinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
64% A solution of copper (II) chloride (173 mg, 1.29 mmol) in acetonitrile (4 mL) was cooled to 0 C., tert-butyl nitrite (199 muL, 1.68 mmol) was added dropwise, and the mixture was stirred at 0 C. for 30 min . A solution of <strong>[116632-57-6]3-bromoquinolin-5-amine</strong> (250 mg, 1.12 mmol) in acetonitrile (4 mL) was added to the reaction solution, and the mixture was stirred at room temperature for 1 hour. 1 N hydrochloric acid was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered, and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (hexane / ethyl acetate) to give the title compound (175 mg, 64%). Light yellow solid
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