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[ CAS No. 205744-17-8 ] {[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| 205744-17-8
Chemical Structure| 205744-17-8
Structure of 205744-17-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 205744-17-8 ]

CAS No. :205744-17-8 MDL No. :MFCD11100747
Formula : C6H7FN2 Boiling Point : -
Linear Structure Formula :- InChI Key :KYRWSLUCAPNJPI-UHFFFAOYSA-N
M.W : 126.13 Pubchem ID :21714708
Synonyms :

Calculated chemistry of [ 205744-17-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.87
TPSA : 38.91 ?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) : -6.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.22
Log Po/w (XLOGP3) : 0.14
Log Po/w (WLOGP) : 0.95
Log Po/w (MLOGP) : 0.31
Log Po/w (SILICOS-IT) : 1.39
Consensus Log Po/w : 0.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.14
Solubility : 9.19 mg/ml ; 0.0729 mol/l
Class : Very soluble
Log S (Ali) : -0.51
Solubility : 38.7 mg/ml ; 0.306 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.31
Solubility : 0.621 mg/ml ; 0.00492 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.62

Safety of [ 205744-17-8 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P260-P264-P280-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405 UN#:2735
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 205744-17-8 ]

* 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.

  • Upstream synthesis route of [ 205744-17-8 ]
  • Downstream synthetic route of [ 205744-17-8 ]

[ 205744-17-8 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 3939-12-6 ]
  • [ 205744-17-8 ]
YieldReaction ConditionsOperation in experiment
85% With ammonia; hydrogen In methanol at 20℃; for 12 h; 6-fluoro-3-cyanopyridine (300 mg, 2.46 mmol)Dissolved in 2 mol / L ammonia / methanol solution (30 mL),Add Raney nickel (0.5g),H2 atmosphere at room temperature for 12 hours.After the reaction, the reaction solution was filtered through diatomaceous earth,Methanol rinse (5 mL x 2),The filtrate is evaporated to dryness,The residue was purified by silica gel column chromatography (dichloromethane: methanol = 100: 4)To give 262 mg of a yellow oily solid,The yield was 85percent.
Reference: [1] Patent: CN106916101, 2017, A, . Location in patent: Paragraph 0149; 0150
[2] Journal of Medicinal Chemistry, 2017, vol. 60, # 19, p. 7965 - 7983
  • 2
  • [ 864061-60-9 ]
  • [ 205744-17-8 ]
Reference: [1] Journal of Fluorine Chemistry, 2005, vol. 126, # 3, p. 345 - 348
  • 3
  • [ 1603-41-4 ]
  • [ 205744-17-8 ]
Reference: [1] Journal of Fluorine Chemistry, 2005, vol. 126, # 3, p. 345 - 348
  • 4
  • [ 2369-19-9 ]
  • [ 205744-17-8 ]
Reference: [1] Journal of Fluorine Chemistry, 2005, vol. 126, # 3, p. 345 - 348
  • 5
  • [ 105827-74-5 ]
  • [ 205744-17-8 ]
Reference: [1] Journal of Fluorine Chemistry, 2005, vol. 126, # 3, p. 345 - 348
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