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[ CAS No. 13544-43-9 ] {[proInfo.proName]}

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Chemical Structure| 13544-43-9
Chemical Structure| 13544-43-9
Structure of 13544-43-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13544-43-9 ]

CAS No. :13544-43-9 MDL No. :MFCD00272316
Formula : C9H6F3N Boiling Point : No data available
Linear Structure Formula :- InChI Key :BPYBYPREOVLFED-UHFFFAOYSA-N
M.W : 185.15 Pubchem ID :2777523
Synonyms :

Calculated chemistry of [ 13544-43-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.3
TPSA : 15.79 ?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) : -4.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 3.84
Log Po/w (WLOGP) : 4.34
Log Po/w (MLOGP) : 2.61
Log Po/w (SILICOS-IT) : 3.48
Consensus Log Po/w : 3.21

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.85
Solubility : 0.0259 mg/ml ; 0.00014 mol/l
Class : Soluble
Log S (Ali) : -3.87
Solubility : 0.0251 mg/ml ; 0.000136 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.17
Solubility : 0.0125 mg/ml ; 0.0000676 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.31

Safety of [ 13544-43-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13544-43-9 ]

* 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 [ 13544-43-9 ]

[ 13544-43-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13544-43-9 ]
  • [ 1677-80-1 ]
  • 1-(3-chloropyridazin-4-yl)-6-trifluoromethyl-1H-indole [ No CAS ]
YieldReaction ConditionsOperation in experiment
Put in a three-necked bottle equipped with nitrogen protection device6-trifluoromethylindole (3.70g, 20mmol), 40ml of N,N-dimethylacetamide, stir and reduce the temperature to below 0,Add 60% sodium hydrogen (0.88g, 22mmol) in batches, keep warm and stir for 0.5 hours,Then add the filtrate of step one dropwise, after the addition, the temperature will rise naturally, and the reaction will be stirred overnight.Add 50ml water, extract three times with ethyl acetate (100ml×3), combine the organic phases,Wash with brine, dry with anhydrous sodium sulfate, and concentrate to dryness under reduced pressure.The concentrate is purified by silica gel chromatography,1-(3-Trichloro-pyridazin-4-yl)-6-trifluoromethyl-1H-indole (Intermediate 1-a) is obtained.
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