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[ CAS No. 147962-81-0 ] {[proInfo.proName]}

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Chemical Structure| 147962-81-0
Chemical Structure| 147962-81-0
Structure of 147962-81-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 147962-81-0 ]

CAS No. :147962-81-0 MDL No. :MFCD11042852
Formula : C10H11BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ILZQYNXOOLMOGA-UHFFFAOYSA-N
M.W : 243.10 Pubchem ID :14945865
Synonyms :

Calculated chemistry of [ 147962-81-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 55.19
TPSA : 26.3 ?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) : -5.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.81
Log Po/w (XLOGP3) : 3.2
Log Po/w (WLOGP) : 2.93
Log Po/w (MLOGP) : 3.25
Log Po/w (SILICOS-IT) : 3.19
Consensus Log Po/w : 3.08

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.51
Solubility : 0.0757 mg/ml ; 0.000311 mol/l
Class : Soluble
Log S (Ali) : -3.42
Solubility : 0.0915 mg/ml ; 0.000377 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.12
Solubility : 0.0183 mg/ml ; 0.0000752 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.81

Safety of [ 147962-81-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 147962-81-0 ]

* 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 [ 147962-81-0 ]

[ 147962-81-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 147962-81-0 ]
  • [ 66521-66-2 ]
  • 4-methyl-3-[[4-(3-pyridyl)-2-pyrimidinyl]amino]benzoic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
45% With copper(l) iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; In 1,4-dioxane; at 100℃; for 20h;Inert atmosphere; Into a three-neck round bottom flask was added raw material compound 5 (0.21 g, 1.2 mmol), and addedsolvent anhydrous 1,4-dioxane 25 mL, catalyst CuI (0.095 g, 0.5 mmol), cocatalyst KI (0.25 g, 1.5). Mmmol),acid binding agent K 2 CO 3 (1.4 g, 2.0 mmol). Then in N 2 The reaction 3-ethyl 4-bromo-4-methylbenzoate(0.243 g, 1.5 mmol) and the ligand DMEDA (60 muL, 0.5 mmol) were added under stirring, and the mixturewas stirred and warmed to 100 C for 20 h. After the reaction was completed, the mixture was cooled to 45 C, and 2 ml of concentrated aqueous ammonia was added to the reaction mixture, and the mixture was stirredfor 30 min, then the system was cooled to room temperature, and the residue was filtered, extracted with ethylacetate 3-4 times, and the organic phases were combined and dried. The mixture was evaporated to dryness,and purified by column chromatography to afford compound 6 (0.15 g, yield: 45%).
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