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[ CAS No. 147754-12-9 ] {[proInfo.proName]}

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Chemical Structure| 147754-12-9
Chemical Structure| 147754-12-9
Structure of 147754-12-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 147754-12-9 ]

CAS No. :147754-12-9 MDL No. :MFCD03095106
Formula : C8H6FN Boiling Point : -
Linear Structure Formula :- InChI Key :BJBXUIUJKPOZLV-UHFFFAOYSA-N
M.W : 135.14 Pubchem ID :3826055
Synonyms :

Calculated chemistry of [ 147754-12-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.08
TPSA : 23.79 ?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) : -5.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.9
Log Po/w (XLOGP3) : 2.11
Log Po/w (WLOGP) : 2.43
Log Po/w (MLOGP) : 2.21
Log Po/w (SILICOS-IT) : 2.68
Consensus Log Po/w : 2.27

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.45
Solubility : 0.478 mg/ml ; 0.00354 mol/l
Class : Soluble
Log S (Ali) : -2.24
Solubility : 0.777 mg/ml ; 0.00575 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.12
Solubility : 0.103 mg/ml ; 0.000762 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.61

Safety of [ 147754-12-9 ]

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

Application In Synthesis of [ 147754-12-9 ]

* 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 [ 147754-12-9 ]

[ 147754-12-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4522-35-4 ]
  • [ 147754-12-9 ]
  • [ 1616069-58-9 ]
YieldReaction ConditionsOperation in experiment
INTERMEDIATE 8 4-(3 -Iodo- lH-p yrazol- 1 - vPbenzonitrile To 3-iodo-lH-pyrazole (801 mg, 4.13 mmol) in DMSO (10 mL) at 0 C, was added sodium hydride (60% in mineral oil, 198 mg, 4.95 mmol). The reaction was warmed to 25 C and stirred for 60 min before methyl 4-fluorobenzonitrile (500 mg, 4.13 mmol) was added. The reaction mixture was stirred at 90 C for 4.5 h before quenching by the addition of water. The reaction mixture was extracted with EtOAc. The combined organic extracts were dried over MgS04 and concentrated in vacuo. The crude mixture was purified by flash chromatography (ISCO Combifiash, 0-30% EtOAc in hexanes) to afford 4-(3-iodo-lH-pyrazol-l-yl)benzonitrile, as a pale yellow crystaline solid. LCMS calc. = 295.96; found = 295.90 (M+H)+. NMR (500 MHz, CDC13): delta 7.83 (m, 3 H); 7.78 (d, J= 8.5 Hz, 2 H), 6.71 (d, J= 2.6 Hz, 1 H).
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