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[ CAS No. 5535-48-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 5535-48-8
Chemical Structure| 5535-48-8
Structure of 5535-48-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5535-48-8 ]

CAS No. :5535-48-8 MDL No. :MFCD00007554
Formula : C8H8O2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :UJTPZISIAWDGFF-UHFFFAOYSA-N
M.W : 168.21 Pubchem ID :79664
Synonyms :

Calculated chemistry of [ 5535-48-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.87
TPSA : 42.52 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.61
Log Po/w (XLOGP3) : 0.99
Log Po/w (WLOGP) : 2.68
Log Po/w (MLOGP) : 1.76
Log Po/w (SILICOS-IT) : 1.43
Consensus Log Po/w : 1.7

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.78
Solubility : 2.8 mg/ml ; 0.0167 mol/l
Class : Very soluble
Log S (Ali) : -1.47
Solubility : 5.68 mg/ml ; 0.0338 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.76
Solubility : 0.292 mg/ml ; 0.00173 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.2

Safety of [ 5535-48-8 ]

Signal Word:Danger Class:8
Precautionary Statements:P261-P280-P305+P351+P338 UN#:1759
Hazard Statements:H302-H315-H317-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5535-48-8 ]

* 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 [ 5535-48-8 ]

[ 5535-48-8 ] Synthesis Path-Downstream   1~10

  • 2
  • [ 5535-48-8 ]
  • (E)-tert-butyl([2-(2-phenylethynyl)phenyl]methylidene})amine [ No CAS ]
  • [ 37993-76-3 ]
  • 3
  • [ 10102-94-0 ]
  • [ 5535-48-8 ]
  • [ 1421592-36-0 ]
  • 4
  • [ 144851-82-1 ]
  • [ 5535-48-8 ]
  • 8-fluoro-3-(phenylsulfonyl)-2,3-dihydroquinolin-4(1H)-one [ No CAS ]
  • 5
  • [ 144851-82-1 ]
  • [ 5535-48-8 ]
  • C16H16FNO4S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium tert-butylate; bis[2-(diphenylphosphino)phenyl] ether; copper(l) chloride; In toluene; at 22℃; for 20h;Inert atmosphere; Sealed tube; General procedure: CuCl (1.50 mg, 0.0150 mmol), DPEPhos (8.10 mg, 0.0150 mmol) and KOt-Bu (1.70 mg,0.0150 mmol) were added to a 8 mL vial charged with a magnetic bar. The vial was sealedwith a cap (phenolic open top cap with gray PTFE/silicone) and purged by N2 gas for 5 min.Toluene (0.8 mL) and methyl 2-aminobenzoate (1a) (46.6 L, 0.360 mmol) were added to themixture, which was allowed for 10 min. And then a solution of phenyl vinyl sulfone (2) (50.5mg, 0.300 mmol) in toluene (0.7 mL) was added to the reaction solution. After stirring atroom temperature for 5 h, THF (5 mL) was added and the reaction was allowed to cool to 0C (ice bath). After addition of KOt-Bu (101 mg, 0.900 mmol), the resulting solution wasallowed to stir for further 1 h at 0 C. After that time, the reaction was quenched with asaturated aqueous solution of NH4Cl (1 mL) and NaHCO3 (2 mL) and washed with EtOAc (7x 3 mL). The organic layers were combined, dried over MgSO4, filtered, and concentrated invacuo. The crude product was purified by silica gel column chromatography (CH2Cl2/EtOAc,8:1) to afford the desired product 4a (76.8 mg, 0.267 mmol, 89% yield) as a yellow solid.
  • 6
  • [ 5535-48-8 ]
  • [ 3839-35-8 ]
  • [ 34009-05-7 ]
  • 7
  • [ 5535-48-8 ]
  • [ 475250-52-3 ]
  • 1-methoxy-4-(3-(phenylsulfonyl)propyl)benzene [ No CAS ]
  • 8
  • [ 5535-48-8 ]
  • [ 20101-92-2 ]
  • (E)-3-(2-carbamoylmethyl-5-chlorophenyl)acrylic acid ethyl ester [ No CAS ]
  • 9
  • [ 5535-48-8 ]
  • [ 39769-09-0 ]
  • C21H17F2NO2S [ No CAS ]
  • C21H17F2NO2S [ No CAS ]
  • 10
  • [ 702-79-4 ]
  • [ 5535-48-8 ]
  • C20H28O2S [ No CAS ]
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