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[ CAS No. 654655-69-3 ] {[proInfo.proName]}

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Chemical Structure| 654655-69-3
Chemical Structure| 654655-69-3
Structure of 654655-69-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 654655-69-3 ]

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Product Citations

Product Details of [ 654655-69-3 ]

CAS No. :654655-69-3 MDL No. :MFCD22493488
Formula : C17H14BrNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :WMFHVNYOCKTDMX-UHFFFAOYSA-N
M.W : 328.20 Pubchem ID :11667032
Synonyms :
Chemical Name :3-Benzyl-6-bromo-2-methoxyquinoline

Calculated chemistry of [ 654655-69-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 16
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 85.39
TPSA : 22.12 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.43
Log Po/w (XLOGP3) : 5.11
Log Po/w (WLOGP) : 4.6
Log Po/w (MLOGP) : 4.14
Log Po/w (SILICOS-IT) : 5.05
Consensus Log Po/w : 4.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.49
Solubility : 0.00107 mg/ml ; 0.00000325 mol/l
Class : Moderately soluble
Log S (Ali) : -5.32
Solubility : 0.00158 mg/ml ; 0.0000048 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.58
Solubility : 0.00000871 mg/ml ; 0.0000000265 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.25

Safety of [ 654655-69-3 ]

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 [ 654655-69-3 ]

* 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 [ 654655-69-3 ]

[ 654655-69-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 654655-69-3 ]
  • [ 21970-65-0 ]
  • C34H33BrN2O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Compound J was prepared as follows: present intermediate 3 was reacted with intermediate compound 3 of WO 2004/011436 in the same way as described in Example B12 of WO 2004/011436. The obtained residue (4.9 g) was purified by column chromatography over silica gel (eluent: CH2Cl2). One fraction was collected and the solvent was evaporated. Yield: 1.43 g of compound J, which is a mixture of diastereoisomers.
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Technical Information

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1-Iodonaphthalene

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