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[ CAS No. 3939-13-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3939-13-7
Chemical Structure| 3939-13-7
Structure of 3939-13-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 3939-13-7 ]

CAS No. :3939-13-7 MDL No. :MFCD03095082
Formula : C6H3FN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :USIDQCCXMGJOJM-UHFFFAOYSA-N
M.W : 122.10 Pubchem ID :2783254
Synonyms :

Calculated chemistry of [ 3939-13-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 28.91
TPSA : 36.68 ?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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.22
Log Po/w (XLOGP3) : 1.0
Log Po/w (WLOGP) : 1.51
Log Po/w (MLOGP) : 0.22
Log Po/w (SILICOS-IT) : 1.76
Consensus Log Po/w : 1.14

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.72
Solubility : 2.32 mg/ml ; 0.019 mol/l
Class : Very soluble
Log S (Ali) : -1.36
Solubility : 5.34 mg/ml ; 0.0437 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.34
Solubility : 0.554 mg/ml ; 0.00454 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.63

Safety of [ 3939-13-7 ]

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

Application In Synthesis of [ 3939-13-7 ]

* 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 [ 3939-13-7 ]

[ 3939-13-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 3939-13-7 ]
  • [ 5271-27-2 ]
  • [ 61337-88-0 ]
  • 2
  • [ 546-88-3 ]
  • [ 3939-13-7 ]
  • [ 92914-74-4 ]
YieldReaction ConditionsOperation in experiment
28% Synthesis of intermediate VX001: Isoxazolo[5,4-b]pyridin-3-amine 909 mg (8.1 mmol) of KO-t-Bu were added, with vigorous stirring, to a suspension of 668 mg (8.9 mmol) of acethydroxamic acid in DMF (20 ml), and the mixture was stirred for 30 min at RT. 990 mg (8.1 mmol) of 2-fluoro-nicotinonitrile were then added, and stirring was carried out for a further 5 h at 50 C. The mixture was then extracted with EA and the organic phase was dried over Na2SO4, filtered and concentrated in vacuo. CC (hexane/EA 7:3) of the residue yielded 305 mg (2.3 mmol, 28%) of isoxazolo[5,4-b]pyridin-3-amine.
  • 3
  • [ 3939-13-7 ]
  • [ 92914-74-4 ]
  • 4
  • [ 3939-13-7 ]
  • [ 20577-27-9 ]
  • [ 92914-74-4 ]
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