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[ CAS No. 51516-67-7 ] {[proInfo.proName]}

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Chemical Structure| 51516-67-7
Chemical Structure| 51516-67-7
Structure of 51516-67-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 51516-67-7 ]

CAS No. :51516-67-7 MDL No. :MFCD00052031
Formula : C10H7ClN4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WIWSALMJHPGFDY-UHFFFAOYSA-N
M.W : 218.64 Pubchem ID :639097
Synonyms :

Calculated chemistry of [ 51516-67-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
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 : 57.69
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) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 2.44
Log Po/w (WLOGP) : 1.99
Log Po/w (MLOGP) : 1.46
Log Po/w (SILICOS-IT) : 1.36
Consensus Log Po/w : 1.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.21
Solubility : 0.135 mg/ml ; 0.000617 mol/l
Class : Soluble
Log S (Ali) : -3.5
Solubility : 0.0686 mg/ml ; 0.000314 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.28
Solubility : 0.115 mg/ml ; 0.000527 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.97

Safety of [ 51516-67-7 ]

Signal Word:Danger Class:
Precautionary Statements:P280-P301+P312+P330-P302+P352-P305+P351+P338+P310 UN#:
Hazard Statements:H302-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 51516-67-7 ]

* 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 [ 51516-67-7 ]

[ 51516-67-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25365-71-3 ]
  • [ 51516-67-7 ]
  • (E)-1-(4-chlorophenyl)-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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