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[ CAS No. 708-25-8 ] {[proInfo.proName]}

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Chemical Structure| 708-25-8
Chemical Structure| 708-25-8
Structure of 708-25-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 708-25-8 ]

CAS No. :708-25-8 MDL No. :MFCD06204339
Formula : C9H8F2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VTNZLYJCCASTNV-UHFFFAOYSA-N
M.W : 186.16 Pubchem ID :21525436
Synonyms :

Calculated chemistry of [ 708-25-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.44
TPSA : 26.3 ?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) : -5.77 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.24
Log Po/w (XLOGP3) : 2.34
Log Po/w (WLOGP) : 2.98
Log Po/w (MLOGP) : 3.09
Log Po/w (SILICOS-IT) : 2.88
Consensus Log Po/w : 2.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.61
Solubility : 0.455 mg/ml ; 0.00244 mol/l
Class : Soluble
Log S (Ali) : -2.53
Solubility : 0.547 mg/ml ; 0.00294 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.44
Solubility : 0.0679 mg/ml ; 0.000365 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.67

Safety of [ 708-25-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 708-25-8 ]

* 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 [ 708-25-8 ]

[ 708-25-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 2991-28-8 ]
  • [ 708-25-8 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid;Reflux; General procedure: To a stirred solution of different benzoic acids (6.42 mmol) in ethanol (3 mL) was added H2SO4 (0.1mL) and heated to reflux for 6-10 h. The reaction mixture was diluted with ethyl acetate followed by water. The organic layer was washed with saturated NaHCO3 followed by water and brine solution. The organic layer was dried over sodium sulphate, filtered and evaporated to obtain the respective ethyl benzoate derivatives.
With sulfuric acid; for 10h;Reflux; General procedure: A mixture of benzoic acid (6.42 mmol), catalytic quantity of conc. H2SO4 in ethanol was heated to reflux for 10 h. The reaction mixture was diluted with ethyl acetate followed by water. The organic layer was washed with saturated NaHCO3 followed by water and brine solution. The organic layer was dried over sodium sulphate, filtered and evaporated to obtain respective ethyl benzoates.
With sulfuric acid; for 10h;Reflux; General procedure: Benzoic acids a-j(8.12 mmol) was dissolved in ethanol (15 mL) and added catalytic qty of conc.H2SO4and heated to reflux for 10 h. Ethanol was evaporated and the obtained residue was diluted with ethylacetate (25 mL). The organic layer was washed with aqueous saturated NaHCO3(3 X 15 mL) followed by water (2 X 15 mL) and brine solution (20 mL). The organic layer was separated, dried over sodium sulphate, filtered and evaporated to obtain respective ethyl benzoates.
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