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[ CAS No. 497258-85-2 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 497258-85-2
Chemical Structure| 497258-85-2
Structure of 497258-85-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 497258-85-2 ]

CAS No. :497258-85-2 MDL No. :MFCD19442808
Formula : C24H46N4O4S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 486.71 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 497258-85-2 ]

Physicochemical Properties

Num. heavy atoms : 33
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.75
Num. rotatable bonds : 14
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 136.39
TPSA : 106.26 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : -15.64
Log Po/w (XLOGP3) : 5.61
Log Po/w (WLOGP) : 5.09
Log Po/w (MLOGP) : 2.14
Log Po/w (SILICOS-IT) : 2.37
Consensus Log Po/w : -0.09

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.69
Solubility : 0.000989 mg/ml ; 0.00000203 mol/l
Class : Moderately soluble
Log S (Ali) : -7.6
Solubility : 0.0000121 mg/ml ; 0.0000000249 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -3.2
Solubility : 0.308 mg/ml ; 0.000632 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 3.83

Safety of [ 497258-85-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P260-P264-P280-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 497258-85-2 ]

* 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 [ 497258-85-2 ]

[ 497258-85-2 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 616-47-7 ]
  • [ 111-83-1 ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
80% With sodium hydrogen sulfate at 110℃; Microwave irradiation;
  • 2
  • [ 64697-40-1 ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; In water; 1-Octyl-3-Methylimidazolium hydrogensulfate ([OMIm][HSO4])[OMIm][HSO4] was prepared from the anion exchange of [OMIm][Cl] with H2SO4 in deionized water. The ionic liquid is then dried under vacuum. 1H NMR chemical shifts (relative to TMS internal standard) and coupling constants J/Hz: delta=8.65 (s, 1H), 7.39 (d, 2H, J=4.19), 4.17 (q, 2H, J=7.4), 3.93 (s, 3H), 1.87 (m, 4H), 1.32 (m, 6H) 0.87 (t, 3H, J=6.53); water content is less than 100 ppm.
  • 3
  • [ 111-85-3 ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: acetonitrile / 72 h / 39.99 °C / Inert atmosphere 2: sulfuric acid / dichloromethane
  • 4
  • 1-octyl-3-methyl-imidazolium bromide [ No CAS ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid In dichloromethane; water at 0℃; for 48h; Reflux;
With sodium hydrogen sulfate at 20℃; for 72h;
With sodium hydrogen sulfate In acetone at 20℃; for 24h;
With potassium hydrogensulfate In isopropyl alcohol at 20℃; for 18h;
With sodium hydrogen sulfate

  • 5
  • [ 111-83-1 ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 0.5 h / Microwave irradiation 2: sodium hydrogen sulfate / 72 h / 20 °C
Multi-step reaction with 2 steps 1: toluene / 32 h / 0 - 70 °C 2: sodium hydrogen sulfate / acetone / 24 h / 20 °C
Multi-step reaction with 2 steps 1: 18 h / 90 °C / Inert atmosphere 2: potassium hydrogensulfate / isopropyl alcohol / 18 h / 20 °C
  • 6
  • [ 616-47-7 ]
  • [ 497258-85-2 ]
YieldReaction ConditionsOperation in experiment
Stage #1: 1-methyl-1H-imidazole at 69.84℃; for 12h; Stage #2: With sulfuric acid In acetonitrile at 69.84℃;
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