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[ CAS No. 1370046-40-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1370046-40-4
Chemical Structure| 1370046-40-4
Structure of 1370046-40-4 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 1370046-40-4 ]

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Product Details of [ 1370046-40-4 ]

CAS No. :1370046-40-4 MDL No. :MFCD31746881
Formula : C19H21N3O3S Boiling Point : -
Linear Structure Formula :- InChI Key :GONIBFCARADPAC-UHFFFAOYSA-N
M.W : 371.45 Pubchem ID :56944939
Synonyms :

Calculated chemistry of [ 1370046-40-4 ]

Physicochemical Properties

Num. heavy atoms : 26
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.26
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 112.0
TPSA : 101.4 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.32
Log Po/w (XLOGP3) : 2.64
Log Po/w (WLOGP) : 2.02
Log Po/w (MLOGP) : 1.73
Log Po/w (SILICOS-IT) : 3.88
Consensus Log Po/w : 2.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.75
Solubility : 0.0658 mg/ml ; 0.000177 mol/l
Class : Soluble
Log S (Ali) : -4.42
Solubility : 0.0141 mg/ml ; 0.000038 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.0
Solubility : 0.00367 mg/ml ; 0.00000989 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.8

Safety of [ 1370046-40-4 ]

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

Application In Synthesis of [ 1370046-40-4 ]

* 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 [ 1370046-40-4 ]

[ 1370046-40-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 85718-09-8 ]
  • [ 1370046-40-4 ]
  • [ 1370046-31-3 ]
YieldReaction ConditionsOperation in experiment
44% In ethanol Reflux; Inert atmosphere; 2.4. General procedure for preparing [Ru(A)2(B)Cl2] (where A = 2,2-bipyridine/1,10-phenanthroline;B = 3,4,5-tri-OCH3-DPC, 4-CH3-DPC, 4-N-(CH3)2-DPC, 4-NO2-DPC, N-BITSZ,PTSZ and PINH) General procedure: To the black microcrystalline cis-Ru(A)2Cl2 (2 mM), excess of ligand B (2.5 mM) wasadded and refluxed in anhydrous ethanol under nitrogen. The initial colored solutionslowly changed to brownish orange at the end of the reaction, which was verified by TLCon silica plates. Excess ethanol was distilled off and silica gel (60-120 mesh) added to thissolution. The final complex was purified by column chromatography using silica gel asstationary phase and chloroform-methanol as mobile phase.
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