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[ CAS No. 58028-76-5 ] {[proInfo.proName]}

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Chemical Structure| 58028-76-5
Chemical Structure| 58028-76-5
Structure of 58028-76-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 58028-76-5 ]

CAS No. :58028-76-5 MDL No. :MFCD00662562
Formula : C11H13NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :GTTAEWVBVHSDLX-UHFFFAOYSA-N
M.W : 191.23 Pubchem ID :2737010
Synonyms :

Calculated chemistry of [ 58028-76-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 57.56
TPSA : 29.54 ?2

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) : -6.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 1.13
Log Po/w (WLOGP) : 0.95
Log Po/w (MLOGP) : 0.76
Log Po/w (SILICOS-IT) : 2.11
Consensus Log Po/w : 1.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.92
Solubility : 2.29 mg/ml ; 0.0119 mol/l
Class : Very soluble
Log S (Ali) : -1.34
Solubility : 8.66 mg/ml ; 0.0453 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.53
Solubility : 0.559 mg/ml ; 0.00292 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 58028-76-5 ]

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 [ 58028-76-5 ]

* 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 [ 58028-76-5 ]

[ 58028-76-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 58028-76-5 ]
  • [ 465514-33-4 ]
YieldReaction ConditionsOperation in experiment
Reference Example 51 (2-Morpholin-4-ylphenyl)methanol 2-Fluorobenzaldehyde (1.0 g, 8.1 mmol) was dissolved in DMF (20 mL), morpholine (2.0 mL) and potassium carbonate (1.1 g, 8.1 mmol) were added thereto, and then the mixture was stirred at 80C for 2 days. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate = 98: 2 to 60: 40) to give an oily matter. The resulting oily matter was dissolved in methanol (20 mL), sodium borohydride (613 mg, 16.2 mmol) was added thereto, and the mixture was stirred at room temperature for 3 hours. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure to give the title compound (474 mg, yield 30%).
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