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[ CAS No. 612845-44-0 ] {[proInfo.proName]}

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Chemical Structure| 612845-44-0
Chemical Structure| 612845-44-0
Structure of 612845-44-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 612845-44-0 ]

CAS No. :612845-44-0 MDL No. :MFCD06201032
Formula : C7H10BNO3 Boiling Point : No data available
Linear Structure Formula :NC5H3(OC2H5)B(OH)2 InChI Key :UONCERAQKBPLML-UHFFFAOYSA-N
M.W : 166.97 Pubchem ID :12012237
Synonyms :

Calculated chemistry of [ 612845-44-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 45.36
TPSA : 62.58 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.43
Log Po/w (WLOGP) : -0.84
Log Po/w (MLOGP) : -0.84
Log Po/w (SILICOS-IT) : -0.92
Consensus Log Po/w : -0.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.32
Solubility : 8.03 mg/ml ; 0.0481 mol/l
Class : Very soluble
Log S (Ali) : -1.31
Solubility : 8.15 mg/ml ; 0.0488 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.44
Solubility : 6.05 mg/ml ; 0.0362 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.23

Safety of [ 612845-44-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 612845-44-0 ]

* 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 [ 612845-44-0 ]

[ 612845-44-0 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 5332-24-1 ]
  • [ 612845-44-0 ]
  • 3-(6-ethoxy-pyridin-3-yl)-quinoline [ No CAS ]
  • 2
  • [ 55849-30-4 ]
  • [ 612845-44-0 ]
  • 3
  • [ 7283-96-7 ]
  • [ 612845-44-0 ]
  • 5-(6-ethoxypyridin-3-yl)-thiophene-2-carbaldehyde [ No CAS ]
  • 4
  • [ 942189-39-1 ]
  • [ 612845-44-0 ]
  • [ 1184174-51-3 ]
YieldReaction ConditionsOperation in experiment
89% With potassium carbonate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In 1,4-dioxane; water; at 90℃; for 18h;Inert atmosphere; Example 11Synthesis of 3-Methoxy-1 -(2-f 4-r°-d -methyl-1 H-F1 ,2,41triazol-3-yl)-phenv?-3.6- dihvdro-2H-pyridin-1 -yl)-2-oxo-ethyl)-pyrrolidine-3-carboxylic acid r3-(6-ethoxy- pyridin-3-yl)-1 H-indazol-5-yll-amide (Example 1) Step 1 : A mixture of <strong>[612845-44-0]6-ethoxypyridine-3-boronic acid</strong> (2.5 g, 14.97 mmol), bromoindazole 3Bl (7.25 g, 14.97 mmol), potassium carbonate (6.2 g, 44.91 mmol), PdCI2(dppf)2.CH2Cl2 (1.22 g, 1.497 mmol), 1 ,4-dioxane (40 ml_) and water (10 rriL), was purged with nitrogen for 15 min at r.t. and then heated at 90 0C for 18 hrs and cooled to r.t. Water (100 ml_) and ethyl acetate (300 ml_) were added. Solids were filtered through Celite. Layers were separated and the separated organic layer was washed with water (100 ml_). The combined organic layers were dried (Na2SO4), filtered and solvents were removed in vacuum. Column purification [Hexanes-ethyl acetate = 9:1 (Wv)] gave Compound 2BU (7 g, 89%).
  • 5
  • [ 1333107-70-2 ]
  • [ 612845-44-0 ]
  • [ 1333107-83-7 ]
  • 6
  • [ 1318261-55-0 ]
  • [ 612845-44-0 ]
  • [ 1318261-70-9 ]
  • 8
  • [ 1252932-00-5 ]
  • [ 612845-44-0 ]
  • [ 1350659-19-6 ]
  • 9
  • [ 1350659-26-5 ]
  • [ 612845-44-0 ]
  • [palladium(II)chloride(PPh3)(η5-C5H5)iron(II)(η5-C5H3(NC5H3C5H3N(OC2H5)))] [ No CAS ]
  • 10
  • [ 1002127-25-4 ]
  • [ 612845-44-0 ]
  • C21H20F3NO3 [ No CAS ]
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