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[ CAS No. 52771-21-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 52771-21-8
Chemical Structure| 52771-21-8
Structure of 52771-21-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 52771-21-8 ]

CAS No. :52771-21-8 MDL No. :MFCD00042406
Formula : C8H5F3O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FQEVHRCPXFKJHF-UHFFFAOYSA-N
M.W : 190.12 Pubchem ID :605139
Synonyms :

Calculated chemistry of [ 52771-21-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.51
TPSA : 26.3 ?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) : -5.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.76
Log Po/w (XLOGP3) : 2.92
Log Po/w (WLOGP) : 3.66
Log Po/w (MLOGP) : 1.59
Log Po/w (SILICOS-IT) : 2.54
Consensus Log Po/w : 2.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.0
Solubility : 0.189 mg/ml ; 0.000996 mol/l
Class : Soluble
Log S (Ali) : -3.13
Solubility : 0.14 mg/ml ; 0.000735 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.98
Solubility : 0.201 mg/ml ; 0.00106 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.32

Safety of [ 52771-21-8 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H227-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 52771-21-8 ]

* 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 [ 52771-21-8 ]

[ 52771-21-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 50823-90-0 ]
  • [ 52771-21-8 ]
  • 2
  • [ 39549-79-6 ]
  • [ 52771-21-8 ]
  • 7-methyl-2-(3-(trifluoromethoxy)phenyl)quinazolin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With sodium hydrogensulfite; In N,N-dimethyl acetamide; at 150℃; General procedure: Sodium hydrogen sulfite (4 mmol) was added to a solution of anthranilamide 1 (2 mmol) and benzaldehyde 2 (2 mmol) in N,N- dimethylacetamide (5 mL). The mixture was heated under continuous stirring at 150 o C for 2-3 h and poured into ice water. The precipitate was then filtered, washed with water followed byethanol, and dried to yield the 2-arylquinazolinones 3-31.#10;#10;
  • 3
  • [ 52771-21-8 ]
  • [ 50823-90-0 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogen; In methanol; at 20℃; for 5h; General procedure: A mixture of 1a (196 mg, 1 mmol) and 1%Pd/Ni bimetallic catalyst9 (60 mg, 30 wt %) in MeOH (10 mL) was stirred underH2 at room temperature and atmospheric pressure (on an atmosphericpressure hydrogenation apparatus) until the absorption of hydrogen ceased(3.5 h). After the catalyst was removed off by a magnetic stirring bar, thesolution was evaporated in a vaporator to give the product 2a
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