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[ CAS No. 60532-63-0 ] {[proInfo.proName]}

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Chemical Structure| 60532-63-0
Chemical Structure| 60532-63-0
Structure of 60532-63-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 60532-63-0 ]

CAS No. :60532-63-0 MDL No. :MFCD12546930
Formula : C25H24N4 Boiling Point : -
Linear Structure Formula :- InChI Key :LNHGLSRCOBIHNV-UHFFFAOYSA-N
M.W : 380.49 Pubchem ID :11825069
Synonyms :

Calculated chemistry of [ 60532-63-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 29
Num. arom. heavy atoms : 24
Fraction Csp3 : 0.04
Num. rotatable bonds : 4
Num. H-bond acceptors : 0.0
Num. H-bond donors : 4.0
Molar Refractivity : 122.37
TPSA : 104.08 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.18
Log Po/w (XLOGP3) : 4.24
Log Po/w (WLOGP) : 4.43
Log Po/w (MLOGP) : 3.82
Log Po/w (SILICOS-IT) : 3.53
Consensus Log Po/w : 3.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.22
Solubility : 0.0023 mg/ml ; 0.00000604 mol/l
Class : Moderately soluble
Log S (Ali) : -6.14
Solubility : 0.000278 mg/ml ; 0.00000073 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -8.5
Solubility : 0.00000121 mg/ml ; 0.0000000032 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.54

Safety of [ 60532-63-0 ]

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

Application In Synthesis of [ 60532-63-0 ]

* 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 [ 60532-63-0 ]

[ 60532-63-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5469-19-2 ]
  • [ 60532-63-0 ]
  • [ 1293383-77-3 ]
YieldReaction ConditionsOperation in experiment
64% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; In toluene; at 80℃; for 42h; c. N,N,,N",N"'-(4,4,,4",4,"-methanetetrayltetrakis(benzene-4, 1 - diyl))tetrakis(2,4,5-trimethyl-N-(2,4,5-trimethylphenyl)aniline) In a dry box, 4,4',4",4"'-methanetetrayltetraaniline (1 .00 g, 3.08 mmol), 1 - <strong>[5469-19-2]bromo-2,4,5-trimethylbenzene</strong> (1 .35 g, 3.67 mmol), tris(tert- butyl)phosphine (0.1 0 g, 0.50 mmol) and Pd2(DBA)3 (0.23 g, 0.25 mmol) were combined in round bottom flask and dissolved in 120 ml of dry toluene. The solution was stirred for a minute and followed by sodium tert- butoxide (2.72 g, 28.33 mmol) and 5 ml of dry toluene. A heating mantle was added and the reaction heated to 80C for 18 hour. More 1 -bromo- 2,4,5-trimethylbenzene (350mg) and NaOtBu (180mg) were added and the reaction stirred at 80C for another 24 hour. The reaction mixture was then cooled to room temperature and filtered, washing with toluene (200 mL). The solvent was removed by rotary evaporation and the residue was re-dissolved in chloroform (40ml_). The crude product was precipitated into methanol (300ml_) and collected (3.3g, 85% pure) by filtration. The crude product was purified further by silica gel column chromatography using a gradient of chloroform in hexanes (5-21 %). Recrystallization from chloroform and ethanol yielded 2.60 g (64%) of product as a pale yellow solid. 1 H NMR (CDCI3) is consistent with structure for Compound 2.
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