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[ CAS No. 179897-94-0 ] {[proInfo.proName]}

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Chemical Structure| 179897-94-0
Chemical Structure| 179897-94-0
Structure of 179897-94-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 179897-94-0 ]

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Product Details of [ 179897-94-0 ]

CAS No. :179897-94-0 MDL No. :MFCD01863526
Formula : C7H8BFO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CCQKIRUMTHHPSX-UHFFFAOYSA-N
M.W : 169.95 Pubchem ID :2782673
Synonyms :

Calculated chemistry of [ 179897-94-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 42.72
TPSA : 49.69 ?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) : -6.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : -0.07
Log Po/w (MLOGP) : 0.43
Log Po/w (SILICOS-IT) : -0.32
Consensus Log Po/w : 0.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.7
Solubility : 3.4 mg/ml ; 0.02 mol/l
Class : Very soluble
Log S (Ali) : -1.53
Solubility : 5.03 mg/ml ; 0.0296 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.69
Solubility : 3.48 mg/ml ; 0.0205 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.03

Safety of [ 179897-94-0 ]

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

Application In Synthesis of [ 179897-94-0 ]

* 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 [ 179897-94-0 ]

[ 179897-94-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 122135-83-5 ]
  • [ 179897-94-0 ]
  • [ 654075-20-4 ]
  • 2
  • [ 179897-94-0 ]
  • [ 72955-97-6 ]
  • 3
  • [ 10323-39-4 ]
  • [ 179897-94-0 ]
  • [ 1609538-42-2 ]
  • 4
  • [ 92001-52-0 ]
  • [ 179897-94-0 ]
  • 6-(5-fluoro-2-methoxyphenyl)-8-methyl-9H-purine [ No CAS ]
  • 5
  • [ 118289-17-1 ]
  • [ 179897-94-0 ]
  • 2-(5-fluoro-2-methoxyphenyl)isonicotinaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
83.4% General procedure: To a 50 mL two-necked flask equipped with magnetic stirrer and condenser was added 2-bromopyridine (1.0 eq), Pd(PPh3)4 (5 mol%), K2CO3 solution (2.0 eq) and toluene under N2 at room temperture. After reacted for 15 min, a solution of the boronic acid (1.2 eq) in EtOH was then added. The reaction mixture was then heated to 95 C and reacted for 4 h. After cooling to room temperature, to the reaction mixture aqueous NH4Cl was added and extracted three times with EtOAc. The organic extracts were then combined, washed with brine, dried with MgSO4 and then concentrated under reduced pressure. The crude product was then purified by silica gel column chromatography(Petroleum ether/EtOAc) to give compounds 1 and 5
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