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[ CAS No. 175278-22-5 ] {[proInfo.proName]}

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Chemical Structure| 175278-22-5
Chemical Structure| 175278-22-5
Structure of 175278-22-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 175278-22-5 ]

CAS No. :175278-22-5 MDL No. :MFCD00205143
Formula : C8H6F3NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :IXJFWBNYFTWBOR-UHFFFAOYSA-N
M.W : 221.13 Pubchem ID :2735951
Synonyms :

Calculated chemistry of [ 175278-22-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 6.0
Num. H-bond donors : 2.0
Molar Refractivity : 44.49
TPSA : 72.55 ?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) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.24
Log Po/w (XLOGP3) : 1.99
Log Po/w (WLOGP) : 3.13
Log Po/w (MLOGP) : 0.1
Log Po/w (SILICOS-IT) : 1.13
Consensus Log Po/w : 1.52

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.56
Solubility : 0.605 mg/ml ; 0.00274 mol/l
Class : Soluble
Log S (Ali) : -3.14
Solubility : 0.16 mg/ml ; 0.000725 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.05
Solubility : 1.98 mg/ml ; 0.00897 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.64

Safety of [ 175278-22-5 ]

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 [ 175278-22-5 ]

* 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 [ 175278-22-5 ]

[ 175278-22-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 175278-22-5 ]
  • [ 64-17-5 ]
  • [ 1260742-02-6 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; for 3h;Reflux; Intermediate Example Int24.01eth l 4-amino-3-(trifluoromethoxy)benzoateTo a stirred solution of 4-amino-3-(trifluoromethoxy)benzoic acid (5.0 g) in ethanol (100 mL) was added thionyl chloride (2.47 mL) at 0 C. The mixture was heated to reflux for 3 h. The solvent was removed in vacuum. The residue was dissolved in ethyl acetate and the mixture was washed with a half- saturated solution of sodium bicarbonate and with saturated sodium chloride solution, dried (sodium sulfate) and the solvent was removed in vacuum, to give 4.81 g of the title compound, that was used for the next step without purification.
With thionyl chloride; In ethanol; for 3h;Reflux; Intermediate Example Int 15.07.01ethyl 4-amino-3-(trifluoromethoxy)benzoate To a stirred solution of 4-amino-3-(trifluoromethoxy)benzoic acid (5.0 g) in ethanol (100 mL) was added thionyl chloride (2.47 mL) at 0 C. The mixture was heated to reflux for 3 h. The solvent was removed in vacuum. The residue was dissolved in ethyl acetate and the mixture was washed with a half- saturated solution of sodium bicarbonate and with saturated sodium chloride solution, dried (sodium sulfate) and the solvent was removed in vacuum, to give 4.81 g of the title compound, that was used for the next step without purification.
  • 2
  • [ 175278-22-5 ]
  • [ 1260742-02-6 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In ethanol; for 3h;Reflux; Intermediate Example Int24.01ethyl 4-amino-3-(trifluoromethoxy)benzoateTo a stirred solution of 4-amino-3-(trifluoromethoxy)benzoic acid (5.0 g) in ethanol (100 mL) was added thionyl chloride (2.47 mL) at 0C. The mixture was heated to reflux for 3 h. The solvent was removed in vacuum. The residue was dissolved in ethyl acetate and the mixture was washed with a half- saturated solution of sodium bicarbonate and with saturated sodium chloride solution, dried (sodium sulfate) and the solvent was removed in vacuum, to give 4.81 g of the title compound, that was used for the next step without purification.
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