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[ CAS No. 41917-83-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 41917-83-3
Chemical Structure| 41917-83-3
Structure of 41917-83-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 41917-83-3 ]

CAS No. :41917-83-3 MDL No. :MFCD09835193
Formula : C10H7F3O Boiling Point : -
Linear Structure Formula :- InChI Key :HYCDCKWWJCPUNT-OWOJBTEDSA-N
M.W : 200.16 Pubchem ID :11171628
Synonyms :

Calculated chemistry of [ 41917-83-3 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.54
TPSA : 17.07 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.45 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 2.91
Log Po/w (WLOGP) : 3.96
Log Po/w (MLOGP) : 3.02
Log Po/w (SILICOS-IT) : 3.51
Consensus Log Po/w : 3.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.03
Solubility : 0.185 mg/ml ; 0.000926 mol/l
Class : Soluble
Log S (Ali) : -2.93
Solubility : 0.236 mg/ml ; 0.00118 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.33
Solubility : 0.0943 mg/ml ; 0.000471 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 41917-83-3 ]

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

Application In Synthesis of [ 41917-83-3 ]

* 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 [ 41917-83-3 ]

[ 41917-83-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1670-14-0 ]
  • [ 41917-83-3 ]
  • [ 1821141-05-2 ]
YieldReaction ConditionsOperation in experiment
83% With oxygen; potassium hydroxide In dimethyl sulfoxide at 120℃; for 12h; Green chemistry; 2.1 General procedure for 3aa General procedure: A mixture of benzamidine hydrochloride 1a (0.25mmol), cinnamaldehyde 2a (0.30mol) and KOH (0.50mmol, 2equiv.) was stirred in DMSO (1.0mL) under 1atm O2 atmosphere at 120°C for 12h. After completion of the reaction (monitored by TLC), water (10mL) was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The combined organic layers were then dried over MgSO4, filtered, and then concentrated in vacuo. The residue was purified by flash chromatography on silica gel to give the desired product 3aa as a white solid (using the mixture of petroleum ether and ethyl acetate as eluents).
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