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[ CAS No. 115170-40-6 ] {[proInfo.proName]}

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Chemical Structure| 115170-40-6
Chemical Structure| 115170-40-6
Structure of 115170-40-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 115170-40-6 ]

CAS No. :115170-40-6 MDL No. :MFCD06659750
Formula : C7H7BrN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UZGNFPCHQUHZAI-UHFFFAOYSA-N
M.W : 199.05 Pubchem ID :21964079
Synonyms :

Calculated chemistry of [ 115170-40-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.03
TPSA : 24.92 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.68
Log Po/w (XLOGP3) : 1.9
Log Po/w (WLOGP) : 1.24
Log Po/w (MLOGP) : 1.65
Log Po/w (SILICOS-IT) : 2.39
Consensus Log Po/w : 1.77

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.72
Solubility : 0.384 mg/ml ; 0.00193 mol/l
Class : Soluble
Log S (Ali) : -2.05
Solubility : 1.79 mg/ml ; 0.00899 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.48
Solubility : 0.0653 mg/ml ; 0.000328 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.83

Safety of [ 115170-40-6 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 115170-40-6 ]

* 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 [ 115170-40-6 ]

[ 115170-40-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3616-56-6 ]
  • [ 86087-24-3 ]
  • [ 115170-40-6 ]
  • [ 162012-70-6 ]
  • 4-dimethylamino-N-(4-(2,3-dihydroindol-1-yl)-7-(((3R)-tetrahydrofuran-3-yl)oxy)quinolin-6-yl)-2-(4-methylpiperazin-1-yl)but-2-enamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
48.7% Intermediate IV andBromo-2,3-dihydro-1H-pyrrolo (2,3-b) pyridine to give d,React with (S) -3-hydroxytetrahydrofuran,A dark yellow solid VId was obtained.The intermediate d with activated carbon,Ferric chloride and hydrazine hydrate reduction,Obtained as an off-white solid VIId.Then VIId and diethyl phosphoric acid condensation,Compound VIIId is obtained,In the condensation with (dimethylamino) acetaldehyde diethyl acetal,The target compound was obtained. Yield: 48.7percent.
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