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[ CAS No. 146141-04-0 ] {[proInfo.proName]}

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Chemical Structure| 146141-04-0
Chemical Structure| 146141-04-0
Structure of 146141-04-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 146141-04-0 ]

CAS No. :146141-04-0 MDL No. :MFCD03095288
Formula : C5H3FIN Boiling Point : -
Linear Structure Formula :- InChI Key :ZDGZTSMMMPDJLS-UHFFFAOYSA-N
M.W : 222.99 Pubchem ID :1519483
Synonyms :

Calculated chemistry of [ 146141-04-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.91
TPSA : 12.89 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.71
Log Po/w (XLOGP3) : 1.64
Log Po/w (WLOGP) : 2.25
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 2.83
Consensus Log Po/w : 2.05

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.81
Solubility : 0.345 mg/ml ; 0.00155 mol/l
Class : Soluble
Log S (Ali) : -1.52
Solubility : 6.68 mg/ml ; 0.0299 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.26
Solubility : 0.122 mg/ml ; 0.000548 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.3

Safety of [ 146141-04-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 146141-04-0 ]

* 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 [ 146141-04-0 ]
  • Downstream synthetic route of [ 146141-04-0 ]

[ 146141-04-0 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 372-47-4 ]
  • [ 22282-75-3 ]
  • [ 146141-04-0 ]
Reference: [1] Tetrahedron, 2016, vol. 72, # 17, p. 2196 - 2205
  • 2
  • [ 372-47-4 ]
  • [ 22282-75-3 ]
  • [ 146141-04-0 ]
Reference: [1] Tetrahedron, 2016, vol. 72, # 17, p. 2196 - 2205
  • 3
  • [ 17282-04-1 ]
  • [ 146141-04-0 ]
YieldReaction ConditionsOperation in experiment
98% With chloro-trimethyl-silane; sodium iodide In 1,4-dioxane at 80℃; Example 230; (3 -Fluoropyridin-2-vi)but-3 -vnyDbenzo [d] oxazole; 230(A) 3 -Fluoro-2-iodopyridine ;To a solution of 2-chloro-3-fluoropyridine (400 mg, 3 mmol) in dioxane (6 mL, 0.5M) was added in one portion chlorotrimethylsilane (652 mg, 6 mmol) and sodium iodide (2.20 g, 15 mmol). The resulting mixture was stirred at 80°C overnight. The reaction mixture was concentrated to afford 660 mg of 3-fluoro-2-iodopyridine (Yield : 98percent) as a yellow oil which was used in the next step without further purification
Reference: [1] Patent: WO2005/123703, 2005, A2, . Location in patent: Page/Page column 223
  • 4
  • [ 22282-75-3 ]
  • [ 146141-04-0 ]
Reference: [1] Journal of Organic Chemistry, 1993, vol. 58, # 27, p. 7832 - 7838
[2] Tetrahedron, 1993, vol. 49, # 1, p. 49 - 64
  • 5
  • [ 372-47-4 ]
  • [ 22282-75-3 ]
  • [ 146141-04-0 ]
Reference: [1] Tetrahedron, 2016, vol. 72, # 17, p. 2196 - 2205
  • 6
  • [ 372-47-4 ]
  • [ 22282-75-3 ]
  • [ 146141-04-0 ]
Reference: [1] Tetrahedron, 2016, vol. 72, # 17, p. 2196 - 2205
  • 7
  • [ 372-47-4 ]
  • [ 146141-04-0 ]
Reference: [1] Tetrahedron, 1993, vol. 49, # 1, p. 49 - 64
[2] Organic Letters, 2010, vol. 12, # 11, p. 2517 - 2519
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