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[ CAS No. 2040-04-2 ] {[proInfo.proName]}

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Chemical Structure| 2040-04-2
Chemical Structure| 2040-04-2
Structure of 2040-04-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2040-04-2 ]

CAS No. :2040-04-2 MDL No. :MFCD00008729
Formula : C10H12O3 Boiling Point : -
Linear Structure Formula :(CH3O)2C6H3COCH3 InChI Key :XEUGKOFTNAYMMX-UHFFFAOYSA-N
M.W : 180.20 Pubchem ID :16267
Synonyms :

Calculated chemistry of [ 2040-04-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.62
TPSA : 35.53 ?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) : -6.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 1.19
Log Po/w (WLOGP) : 1.91
Log Po/w (MLOGP) : 1.13
Log Po/w (SILICOS-IT) : 2.19
Consensus Log Po/w : 1.69

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.85
Solubility : 2.54 mg/ml ; 0.0141 mol/l
Class : Very soluble
Log S (Ali) : -1.53
Solubility : 5.29 mg/ml ; 0.0294 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.99
Solubility : 0.186 mg/ml ; 0.00103 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.34

Safety of [ 2040-04-2 ]

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 [ 2040-04-2 ]

* 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 [ 2040-04-2 ]

[ 2040-04-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 917-64-6 ]
  • [ 16932-49-3 ]
  • [ 2040-04-2 ]
  • 2
  • [ 2040-04-2 ]
  • [ 5572-94-1 ]
  • C15H13IO2 [ No CAS ]
  • 3
  • [ 2040-04-2 ]
  • [ 676593-23-0 ]
  • C17H16O2 [ No CAS ]
  • 4
  • [ 2040-04-2 ]
  • [ 5900-59-4 ]
  • 7-chloro-2-(2,6-dimethoxybenzoyl)quinazolin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
50% With iodine; In dimethyl sulfoxide; at 110℃; for 12h; General procedure: DMSO (3 mL) was added to a mixture of acetophenone (1.0equiv.) and I2 (1.1 equiv.). The solutionwas stirred at 110 °C, then 2-aminobenzamide (1.0 equiv.) in 2mL DMSO was added dropwise tothe mixture during 1-2 h. After a complete disappearance of thestarting material, 50 mL water and 30 mL saturated brine wereadded to the mixture. The solution was extracted with CH2Cl2(50 mLx3). The organic layer was washed with 10percent Na2S2O3 solution, dried over anhydrous Na2SO4 and concentrated underreduced pressure. The residue was purified by silica gel chromatography(petroleum ether/EtOAc 5:1) to yield the desiredproducts 9a-9d.
  • 5
  • [ 2040-04-2 ]
  • [ 2734-70-5 ]
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