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[ CAS No. 449758-17-2 ] {[proInfo.proName]}

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Chemical Structure| 449758-17-2
Chemical Structure| 449758-17-2
Structure of 449758-17-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 449758-17-2 ]

CAS No. :449758-17-2 MDL No. :MFCD11044692
Formula : C8H12N2O Boiling Point : -
Linear Structure Formula :- InChI Key :IMZWSOSYNFVECD-UHFFFAOYSA-N
M.W : 152.19 Pubchem ID :21866310
Synonyms :

Calculated chemistry of [ 449758-17-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.62
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.69
TPSA : 27.05 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.87
Log Po/w (XLOGP3) : 1.0
Log Po/w (WLOGP) : 1.26
Log Po/w (MLOGP) : 0.94
Log Po/w (SILICOS-IT) : 1.11
Consensus Log Po/w : 1.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.68
Solubility : 3.15 mg/ml ; 0.0207 mol/l
Class : Very soluble
Log S (Ali) : -1.16
Solubility : 10.6 mg/ml ; 0.0697 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.29
Solubility : 7.81 mg/ml ; 0.0513 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.71

Safety of [ 449758-17-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 449758-17-2 ]

* 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 [ 449758-17-2 ]

[ 449758-17-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 449758-17-2 ]
  • [ 376584-63-3 ]
YieldReaction ConditionsOperation in experiment
48% With n-butyllithium; triisopropylborane; In tetrahydrofuran; hexane; at -78 - 20℃; for 5h; To a cooled solution (-780C) of l-(tetrahydro-pyran-2-yl)-lH-pyrazole (7.6g,52mmol) in THF (5OmL), "BuLi (33mL, 2.5M in hexane, 82.5mmol) and triisopropyl borane (12.7mL, 55mmol) are added dropwise maintaining the temperature at -7O0C. The reaction mixture is stirred at -7O0C for one hour and then allowed to reach room temperature over 4 hours. After quenching the reaction with 2M HCl, the solvent is removed in vacuo and the pH is adjusted to pH 6 using IM NaOH. A precipitate is formed, collected by filtration and washed with toluene and petroleum ether. Trituration with ethyl acetate affords the target compound as a white solid (2.7g, 48percent), which is used in the next step without further purification.
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