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[ CAS No. 313-12-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 313-12-2
Chemical Structure| 313-12-2
Structure of 313-12-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 313-12-2 ]

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Product Details of [ 313-12-2 ]

CAS No. :313-12-2 MDL No. :MFCD00274210
Formula : C8H6F3NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UNLVJVQEDSDPIN-UHFFFAOYSA-N
M.W : 205.13 Pubchem ID :604569
Synonyms :

Calculated chemistry of [ 313-12-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 42.81
TPSA : 63.32 ?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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.38
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 3.15
Log Po/w (MLOGP) : 0.95
Log Po/w (SILICOS-IT) : 1.55
Consensus Log Po/w : 1.85

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.68
Solubility : 0.426 mg/ml ; 0.00208 mol/l
Class : Soluble
Log S (Ali) : -3.16
Solubility : 0.141 mg/ml ; 0.000686 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.3
Solubility : 1.02 mg/ml ; 0.00497 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.4

Safety of [ 313-12-2 ]

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

Application In Synthesis of [ 313-12-2 ]

* 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 [ 313-12-2 ]

[ 313-12-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 391-12-8 ]
  • [ 313-12-2 ]
YieldReaction ConditionsOperation in experiment
With dihydrogen peroxide; In sodium hydroxide; water; A. 3-Trifluoromethyl-2-aminobenzoic acid 7-Trifluoromethylisatin (10 g, 46 mmol) was dissolved in 5percent sodium hydroxide solution (83 ml). To this was added dropwise over 30 minutes a solution of 50percent hydrogen peroxide (7.4 ml) in water (4.6 ml); the temperature rose to 50°. The solution was stirred an additional 30 minutes, acidified (conc. HCl) to pH 1-2, and the tan product was filtered.
  • 2
  • [ 67-56-1 ]
  • [ 391-12-8 ]
  • [ 313-12-2 ]
  • [ 64321-95-5 ]
  • 3
  • [ 313-12-2 ]
  • [ 766473-89-6 ]
YieldReaction ConditionsOperation in experiment
Step A: Preparation of 2-lodo-3-(trifluoromethyl)benzoic acid; [0422] 30% H2SO4 (30 mL) was added to a solution of 3-(trifluoromethyl)anthranilic acid (10.0 g, 48.8 mmol) in DMSO (10 mL) at room temperature. The mixture was cooled to O0C, and a solution of sodium nitrite (5.05 g, 73.2 mmol) in water (10 mL) was added dropwise over 5 minutes. The mixture was stirred for 1 hour at 00C, and a solution of KI in water (10 mL) was added dropwise over 5 minutes. The ice bath was removed, and the mixture was stirred for 1 hour. EtOAc was added, and the solution was washed with 2N sodium nitrite twice, brine once, and dried over MgSO4. The solvent was then removed under vacuum to give the product as an off-white solid (12.6 g). [M- H]- = 315.2.
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