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[ CAS No. 5334-43-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5334-43-0
Chemical Structure| 5334-43-0
Structure of 5334-43-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5334-43-0 ]

CAS No. :5334-43-0 MDL No. :MFCD00020730
Formula : C10H8N4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MAKQREKUUHPPIS-UHFFFAOYSA-N
M.W : 184.20 Pubchem ID :79256
Synonyms :

Calculated chemistry of [ 5334-43-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 52.68
TPSA : 67.63 ?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) : -6.14 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.74
Log Po/w (XLOGP3) : 1.81
Log Po/w (WLOGP) : 1.33
Log Po/w (MLOGP) : 0.9
Log Po/w (SILICOS-IT) : 0.74
Consensus Log Po/w : 1.3

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.64
Solubility : 0.424 mg/ml ; 0.0023 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.26 mg/ml ; 0.00141 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.65
Solubility : 0.409 mg/ml ; 0.00222 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.9

Safety of [ 5334-43-0 ]

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

Application In Synthesis of [ 5334-43-0 ]

* 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 [ 5334-43-0 ]

[ 5334-43-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 41042-12-0 ]
  • [ 5334-43-0 ]
  • [ 124-41-4 ]
  • 2-(4-methoxy-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-N-propylaniline [ No CAS ]
YieldReaction ConditionsOperation in experiment
59% In methanol;Reflux; General procedure: A 2 M solution of MeONa in MeOH (2.5 ml, 5 mmol) wasadded to a mixture of 5-amino-1-phenyl-1-pyrazolo-4-carbonitrile (4) (460 mg, 2.5 mmol) and the appropriateN-substituted isatin 2a-d (2.5 mmol) in MeOH (15-20 ml).The reaction mixture was refluxed for 9-11 h (control byTLC). The precipitate that formed after cooling was filteredoff and recrystallized from 2-PrOH.
  • 2
  • [ 25365-71-3 ]
  • [ 5334-43-0 ]
  • (E)-1-phenyl-5-(((2-phenyl-1H-indol-3-yl)methylene)amino)-1H-pyrazole-4-carbonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In ethanol; water; at 80℃; General procedure: Intermediate 4 (1mmol) and the intermediate 7 (1mmol) were dissolved in ethanol to the glass flask, then HCl solution was added as a catalyst refluxed at 80C for 15-18h. After the TLC monitoring reaction was completed, the mixture was vacuum filtered and concentrated. Finally, the above crude product can be isolated and purified by column chromatography (Hexane/EtOAc=8:1) to obtain target compounds.
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