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[ CAS No. 17639-64-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 17639-64-4
Chemical Structure| 17639-64-4
Structure of 17639-64-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 17639-64-4 ]

CAS No. :17639-64-4 MDL No. :MFCD00145014
Formula : C11H11NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :OXWIEWFMRVJGNY-UHFFFAOYSA-N
M.W : 221.28 Pubchem ID :640087
Synonyms :

Calculated chemistry of [ 17639-64-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.09
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 58.47
TPSA : 47.45 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.05 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.18
Log Po/w (XLOGP3) : 2.26
Log Po/w (WLOGP) : 3.11
Log Po/w (MLOGP) : 2.37
Log Po/w (SILICOS-IT) : 1.28
Consensus Log Po/w : 2.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.05
Solubility : 0.199 mg/ml ; 0.000899 mol/l
Class : Soluble
Log S (Ali) : -2.89
Solubility : 0.283 mg/ml ; 0.00128 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.62
Solubility : 0.0532 mg/ml ; 0.00024 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 17639-64-4 ]

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

Application In Synthesis of [ 17639-64-4 ]

* 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 [ 17639-64-4 ]

[ 17639-64-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17639-64-4 ]
  • [ 104-21-2 ]
  • [ 1575721-36-6 ]
YieldReaction ConditionsOperation in experiment
88% With proton-exchanged montmorillonite; In dichloromethane;Reflux; General procedure: To a mixture of arene or heteroarene (0.549 mmol) and 12(66 mg, 0.366 mmol) in anhydrous CH2Cl2 (3 mL) was added Hmont(260 mg). The reaction mixture was stirred at room temperatureor under reflux temperature until the TLC indicated theconsumption of the starting material. The mixture was filtered toremove H-mont, and the filtrate was evaporated under reducedpressure. The residue was purified by flash chromatography (petroleumether/ethyl acetate 200:1 to 10:1) to give the product.Following the procedure, 14a,b and 14h,i were prepared.
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