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[ CAS No. 104863-67-4 ] {[proInfo.proName]}

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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 104863-67-4
Chemical Structure| 104863-67-4
Structure of 104863-67-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 104863-67-4 ]

CAS No. :104863-67-4 MDL No. :MFCD00077565
Formula : C4H6F3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :JDBJZZTZYKUFFK-UHFFFAOYSA-N
M.W : 157.09 Pubchem ID :2782382
Synonyms :

Calculated chemistry of [ 104863-67-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 25.71
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) : -6.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.47
Log Po/w (XLOGP3) : 0.89
Log Po/w (WLOGP) : 1.83
Log Po/w (MLOGP) : 0.61
Log Po/w (SILICOS-IT) : 0.21
Consensus Log Po/w : 1.0

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.18
Solubility : 10.5 mg/ml ; 0.0666 mol/l
Class : Very soluble
Log S (Ali) : -1.1
Solubility : 12.6 mg/ml ; 0.0803 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.55
Solubility : 44.0 mg/ml ; 0.28 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.81

Safety of [ 104863-67-4 ]

Signal Word:Danger Class:3,6.1
Precautionary Statements:P301+P310-P305+P351+P338 UN#:1992
Hazard Statements:H225-H301-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 104863-67-4 ]

* 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 [ 104863-67-4 ]

[ 104863-67-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 100342-30-1 ]
  • [ 104863-67-4 ]
  • 5-(2,2,2-Trifluoro-acetyl)-thiophene-2-sulfonic acid tert-butylamide [ No CAS ]
  • 2
  • 1,3-dichloro-2-fluoro-5-iodo-benzene [ No CAS ]
  • [ 104863-67-4 ]
  • [ 1190865-44-1 ]
YieldReaction ConditionsOperation in experiment
53% With n-butyllithium; In tetrahydrofuran; hexane; at -78℃; for 0.333333h; To a solution of 1 ,3-dichloro-2-fluoro-5-iodo-benzene (CAS 133307-08-1 , 50 g) and 2,2,2-trifluoro-/S/-methoxy-/S/-methyl-acetamide (40.5 g) in THF (800 ml.) at -78C was added n-BuLi (82.5 ml_, 2.5 M in hexanes). The reaction was stirred for 20 min, then quenched by saturated aqueous NH4CI solution and extracted with ethyl acetate. The organic layer was dried (Na2S04), filtered, and concentrated. The residue was purified by flash chromatography on silica gel to afford the product (24 g, 53%). H NMR (400 MHz, CDC ): delta 8.0 (m, 2H).
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