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[ CAS No. 1263314-16-4 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1263314-16-4
Chemical Structure| 1263314-16-4
Chemical Structure| 1263314-16-4
Structure of 1263314-16-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1263314-16-4 ]

CAS No. :1263314-16-4 MDL No. :MFCD11846228
Formula : C7H8Cl2N2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :GHQHLNPDZLZVLB-UHFFFAOYSA-N
M.W : 255.12 Pubchem ID :71303236
Synonyms :

Calculated chemistry of [ 1263314-16-4 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.92
TPSA : 68.3 Ų

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) : -6.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.82
Log Po/w (XLOGP3) : 2.49
Log Po/w (WLOGP) : 2.83
Log Po/w (MLOGP) : 0.98
Log Po/w (SILICOS-IT) : 2.27
Consensus Log Po/w : 2.08

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.18
Solubility : 0.17 mg/ml ; 0.000667 mol/l
Class : Soluble
Log S (Ali) : -3.57
Solubility : 0.0688 mg/ml ; 0.00027 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.99
Solubility : 0.0259 mg/ml ; 0.000101 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.13

Safety of [ 1263314-16-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H320-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1263314-16-4 ]

* 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 [ 1263314-16-4 ]

[ 1263314-16-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1263314-13-1 ]
  • [ 1263314-16-4 ]
YieldReaction ConditionsOperation in experiment
90% With potassium peroxymonosulfate sulfate; tetrabutylammomium bromide In water; acetone at 20℃; General procedure for the synthesis of 2-(methylsulfonyl)pyrimidines (5a-5h) General procedure: A mixture of 2-(methylthio)pyrimidines (5 mmol), tetrabutylammonium bromide (0.16 g, 0.5 mmol, 10 mol%) and acetone (20 mL) was stirred at room temperature. The Oxone (12.5 mmol, 2.5 equiv) in water (20 mL) was added slowly to the vigorously stirred solution. After 4-6 h, TLC indicated the consumption of the starting material. The products 5 were isolated by filtering through a Buechner funnel and washed with water, and then dried to give the solid product. Yields, melting points and spectroscopic data for selected 2-(methylsulfonyl)pyrimidines are listed as follows.
  • 2
  • [ 133-13-1 ]
  • [ 1263314-16-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: sodium hydroxide / ethanol / 4 h / Reflux 2: trichlorophosphate; triethylamine / 3 h / Reflux 3: tetrabutylammomium bromide; potassium peroxymonosulfate sulfate / acetone; water / 20 °C
  • 3
  • [ 42039-70-3 ]
  • [ 1263314-16-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: trichlorophosphate; triethylamine / 3 h / Reflux 2: tetrabutylammomium bromide; potassium peroxymonosulfate sulfate / acetone; water / 20 °C
Same Skeleton Products
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