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[ CAS No. 1063733-41-4 ] {[proInfo.proName]}

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Chemical Structure| 1063733-41-4
Chemical Structure| 1063733-41-4
Structure of 1063733-41-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1063733-41-4 ]

CAS No. :1063733-41-4 MDL No. :MFCD20784227
Formula : C11H13N3O2S Boiling Point : -
Linear Structure Formula :- InChI Key :ZEZFQTOAJHHYCZ-UHFFFAOYSA-N
M.W : 251.31 Pubchem ID :57732216
Synonyms :

Calculated chemistry of [ 1063733-41-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.27
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 66.69
TPSA : 84.51 ?2

Pharmacokinetics

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

Lipophilicity

Log Po/w (iLOGP) : 2.71
Log Po/w (XLOGP3) : 2.51
Log Po/w (WLOGP) : 1.82
Log Po/w (MLOGP) : 0.3
Log Po/w (SILICOS-IT) : 2.67
Consensus Log Po/w : 2.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.13
Solubility : 0.187 mg/ml ; 0.000744 mol/l
Class : Soluble
Log S (Ali) : -3.93
Solubility : 0.0295 mg/ml ; 0.000117 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.16
Solubility : 0.0175 mg/ml ; 0.0000698 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.36

Safety of [ 1063733-41-4 ]

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 [ 1063733-41-4 ]

* 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 [ 1063733-41-4 ]

[ 1063733-41-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1063733-41-4 ]
  • [ 192945-49-6 ]
  • C20H19N5O6S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
General procedure: Under the protection of nitrogen at -10 ,Sulfonyl chloride (6.15mL, 76.132mmol) in anhydrous dichloromethane (60mL)The solution was slowly added dropwise to a solution of DIPEA (24.6g, 190.330mmol) in dry methylene chloride (80mL), slowly warmed to room temperature and reacted for 30 minutes,N- (2,4-dimethoxybenzyl) -1,2,4-thiadiazol-5-amine (9.57g, 38.066mmol) was added, the temperature was raised to reflux for 10 hours, and the solvent was distilled off under reduced pressureThe residue was dissolved in acetonitrile (100mL) and added at 0 C4-bromo-1H-indazole (5.0g, 25.377mmmol) and anhydrous potassium carbonate (7.72g, 55.829mmol), heated to 60 for 20 hours, after the reaction,It was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate (300 mL), washed with water (90 mL x 2), saturated ammonium chloride solution (90 mL x 2), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. Silica gel column chromatography purification (eluent: petroleum ether / ethyl acetate = 6: 1v / v),4-Bromo-N- (2,4-dimethoxybenzyl) -N- (1,2,4-thiadiazol-5-yl) -1H-indazole-1-benzenesulfonamide was obtained, Rate 20.4%,
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