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[ CAS No. 62584-23-0 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 62584-23-0
Chemical Structure| 62584-23-0
Chemical Structure| 62584-23-0
Structure of 62584-23-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 62584-23-0 ]

CAS No. :62584-23-0 MDL No. :MFCD04115832
Formula : C8H5ClF3NO Boiling Point : -
Linear Structure Formula :- InChI Key :PIYDLRBTABXQSP-UHFFFAOYSA-N
M.W : 223.58 Pubchem ID :3770849
Synonyms :

Calculated chemistry of [ 62584-23-0 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.55
TPSA : 43.09 Ų

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) : -5.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.46
Log Po/w (XLOGP3) : 3.03
Log Po/w (WLOGP) : 3.61
Log Po/w (MLOGP) : 2.83
Log Po/w (SILICOS-IT) : 2.67
Consensus Log Po/w : 2.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.32
Solubility : 0.107 mg/ml ; 0.000478 mol/l
Class : Soluble
Log S (Ali) : -3.6
Solubility : 0.0561 mg/ml ; 0.000251 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.5
Solubility : 0.0712 mg/ml ; 0.000318 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 62584-23-0 ]

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 [ 62584-23-0 ]

* 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 [ 62584-23-0 ]

[ 62584-23-0 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 62584-23-0 ]
  • N-(3-(1H-pyrrol-2-ylmethylidene)-2-oxoindolin-6-ylcarbamoyl)-4-chloro-3-(trifluoromethyl)benzamide [ No CAS ]
  • 3
  • [ 62584-23-0 ]
  • [ 1621584-40-4 ]
  • 4
  • [ 79-37-8 ]
  • [ 62584-23-0 ]
  • [ 1513850-32-2 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 40.0℃; General procedure: Oxalyl chloride (6.61mmol) was added dropwise into a stirred solution of the appropriate benzamide (2.6mmol) in CH2Cl2 (10mL). The mixtures were heated at reflux for 20-22h. Then, solvents were evaporated in vacuo to give the respective crude benzoyl isocyanates 4a-k, which were used immediately in the next step without purification. Aminoindolin-2-one (2.8mmol) was added into a stirred solution of the appropriate benzoyl isocyanate (2.8mmol) in acetonitrile (10mL). After addition, each mixture was heated at 70-80C for 2-3h. The solid products were each filtered, washed with acetonitrile, and air dried.
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