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[ CAS No. 599-66-6 ] {[proInfo.proName]}

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Chemical Structure| 599-66-6
Chemical Structure| 599-66-6
Structure of 599-66-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 599-66-6 ]

CAS No. :599-66-6 MDL No. :MFCD00041332
Formula : C14H14O2S Boiling Point : -
Linear Structure Formula :C6H4SO2C7H7CH3 InChI Key :WEAYCYAIVOIUMG-UHFFFAOYSA-N
M.W : 246.32 Pubchem ID :69030
Synonyms :

Calculated chemistry of [ 599-66-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 68.31
TPSA : 42.52 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.35 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 3.45
Log Po/w (WLOGP) : 4.22
Log Po/w (MLOGP) : 3.6
Log Po/w (SILICOS-IT) : 3.28
Consensus Log Po/w : 3.42

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.93
Solubility : 0.0289 mg/ml ; 0.000117 mol/l
Class : Soluble
Log S (Ali) : -4.02
Solubility : 0.0233 mg/ml ; 0.0000946 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.62
Solubility : 0.000591 mg/ml ; 0.0000024 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.88

Safety of [ 599-66-6 ]

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

Application In Synthesis of [ 599-66-6 ]

* 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 [ 599-66-6 ]

[ 599-66-6 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 620-94-0 ]
  • [ 599-66-6 ]
YieldReaction ConditionsOperation in experiment
98% With Octanoic acid; dihydrogen peroxide; In acetonitrile; at 50℃; for 0.5h;Schlenk technique; Green chemistry; General procedure: An oven-dried Schlenk flask was allowed to cool toroom temperature and charged sequentially with sulfide(1.0 mmol), MeCN (3.0 mL) and caprylic acid (20 mol%).The reaction was then activated by the addition of 30%H2O2 (2.4 equiv.) and stirred at 50 C for the required timeas given in Table 4. The progress of reaction was monitoredby GC. After completion of the reaction, the reaction was quenched by adding aqueous solution of 10% Na2SO3to the reaction mixture. Then the product was extractedwith CH2Cl2 (30 mL) and then washed with distilled water(10 mL). The organic extract dried over Na2SO4 and thesolvent removed under reduced pressure. The resultantproduct was purified (if necessary) by column chromatographyusing silica gel (60-120 mesh) with n-hexaneand ethyl acetate as solvent to get the pure product. Thestructure of the product was confirmed by GC-MS, M.P./B.P. and 1H NMR spectroscopic techniques.
  • 2
  • [ 599-66-6 ]
  • [ 1235-89-8 ]
  • 5
  • [ 599-66-6 ]
  • bis-(4-dibromomethyl-phenyl)-sulfone [ No CAS ]
  • 7
  • [ 1774-35-2 ]
  • [ 599-66-6 ]
Reference: [1]Russian Journal of Organic Chemistry,1995,vol. 31,p. 1520 - 1525
    Zhurnal Organicheskoi Khimii,1995,vol. 31,p. 1692 - 1697
[2]Journal of Organic Chemistry,1983,vol. 48,p. 3585 - 3587
[3]Journal of Organic Chemistry,2007,vol. 72,p. 5847 - 5850
[4]Canadian Journal of Chemistry,1984,vol. 62,p. 1164 - 1168
[5]Journal of the American Chemical Society,1946,vol. 68,p. 973,974, 976, 2671
    Journal of the American Chemical Society,1947,vol. 69,p. 644,2310
[6]Magnetic Resonance in Chemistry,1989,vol. 27,p. 360 - 367
[7]Journal of the Chemical Society. Chemical communications,1982,p. 1352 - 1353
[8]Journal of the American Chemical Society,1981,vol. 103,p. 3832 - 3837
[9]Canadian Journal of Chemistry,1987,vol. 65,p. 2421 - 2424
[10]Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical,1981,vol. 20,p. 505 - 506
[11]Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical,1986,vol. 25,p. 678 - 680
[12]Journal of the Indian Chemical Society,1992,vol. 69,p. 819 - 821
[13]Journal of Organic Chemistry,1993,vol. 58,p. 5055 - 5059
[14]Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical,1989,vol. 28,p. 250 - 252
[15]Tetrahedron,2001,vol. 57,p. 1369 - 1374
[16]Journal of Chemical Research, Miniprint,2000,p. 1118 - 1133
[17]Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical,2005,vol. 44,p. 71 - 75
[18]Journal of the Indian Chemical Society,2007,vol. 84,p. 679 - 682
  • 8
  • [ 6311-23-5 ]
  • [ 599-66-6 ]
  • [ 141368-26-5 ]
  • 9
  • [ 114190-45-3 ]
  • [ 599-66-6 ]
  • [ 335305-93-6 ]
  • 10
  • [ 6192-52-5 ]
  • [ 599-66-6 ]
  • 11
  • [ 599-66-6 ]
  • [ 108-24-7 ]
  • [ 64-19-7 ]
  • bis-(4-diacetoxymethyl-phenyl)-sulfone [ No CAS ]
  • 13
  • [ 104-15-4 ]
  • [ 599-66-6 ]
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