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[ CAS No. 157662-77-6 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 157662-77-6
Chemical Structure| 157662-77-6
Chemical Structure| 157662-77-6
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Product Details of [ 157662-77-6 ]

CAS No. :157662-77-6 MDL No. :MFCD09909410
Formula : C8H5FN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :FCOLUCPHJHRTLY-UHFFFAOYSA-N
M.W : 180.14 Pubchem ID :11458029
Synonyms :

Calculated chemistry of [ 157662-77-6 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.74
TPSA : 69.61 Ų

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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : 1.51
Log Po/w (WLOGP) : 2.22
Log Po/w (MLOGP) : 1.83
Log Po/w (SILICOS-IT) : 0.4
Consensus Log Po/w : 1.41

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.12
Solubility : 1.37 mg/ml ; 0.00763 mol/l
Class : Soluble
Log S (Ali) : -2.58
Solubility : 0.474 mg/ml ; 0.00263 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.55
Solubility : 0.511 mg/ml ; 0.00284 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 157662-77-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 157662-77-6 ]

* 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 [ 157662-77-6 ]
  • Downstream synthetic route of [ 157662-77-6 ]

[ 157662-77-6 ] Synthesis Path-Upstream   1~12

  • 1
  • [ 13435-20-6 ]
  • [ 15017-52-4 ]
  • [ 157662-77-6 ]
YieldReaction ConditionsOperation in experiment
80% at 20℃; for 4 h; 34A: 2-(4-fluoro-3-nitrophenyl)acetonitrile To a solution of 4-(bromomethyl)-l-fluoro-2-nitrobenzene (1 g, 4.27 mmol) in acetonitrile (5 mL) was added tetraethylammonium cyanide (0.801 g, 5.13 mmol). The resulting deep green solution was stirred at RT for 4 h. The solvent was then removed in vacuo, purification via flash chromatography gave 34A (light yellow oil, 617 mg, 3.43 mmol, 80 percent yield). LC-MS Anal. Calc'd for C8H5F 2O2 180.03, did not show paretn ion, Tr = 0.74 min (Method B).
Reference: [1] Patent: WO2014/150646, 2014, A1, . Location in patent: Page/Page column 76; 77
[2] Journal of the Chemical Society - Series Chemical Communications, 1994, # 4, p. 439 - 440
  • 2
  • [ 15017-52-4 ]
  • [ 157662-77-6 ]
YieldReaction ConditionsOperation in experiment
47% With 18-crown-6 ether; potassium iodide In N,N-dimethyl-formamide at 20℃; A mixture of 4-(bromomethyl)-1 -fluoro-2-nitrobenzene (18 g, 76.9 mmol), KCN (10 g, 153.8 mmol), Kl (1 .3 g, 7.69 mmol) and 18-Crown-6 (10 g, 38.5 mmol) in DMF (100 mL) was stirred at r.t. overnight. The resulting mixture was partitioned between EtOAc and H20. The organic layer was washed with brine, dried over Na2S04, filtered and concentrated to give the crude product which was purified by flash chromatography (silica gel, 0-30percent EtOAc in PE) to afford the title compound (6.6 g, 47percent yield). LCMS (ESI) m/z calcd for C8H5FN202: 180.03. Found: 181 .37 (M+1)+.
Reference: [1] Patent: WO2018/116107, 2018, A1, . Location in patent: Page/Page column 273-274
  • 3
  • [ 20274-69-5 ]
  • [ 157662-77-6 ]
Reference: [1] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5535 - 5542
[2] Journal of the Chemical Society - Series Chemical Communications, 1994, # 4, p. 439 - 440
[3] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 4, p. 1131 - 1132
[4] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 4, p. 1131 - 1132
  • 4
  • [ 459-22-3 ]
  • [ 157662-77-6 ]
Reference: [1] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 4, p. 1131 - 1132
  • 5
  • [ 15017-52-4 ]
  • [ 157662-77-6 ]
Reference: [1] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5535 - 5542
  • 6
  • [ 42564-51-2 ]
  • [ 157662-77-6 ]
Reference: [1] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5535 - 5542
[2] Journal of the Chemical Society - Series Chemical Communications, 1994, # 4, p. 439 - 440
  • 7
  • [ 446-11-7 ]
  • [ 157662-77-6 ]
Reference: [1] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5535 - 5542
  • 8
  • [ 459-57-4 ]
  • [ 157662-77-6 ]
Reference: [1] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5535 - 5542
  • 9
  • [ 773837-37-9 ]
  • [ 15017-52-4 ]
  • [ 157662-77-6 ]
Reference: [1] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 4, p. 1131 - 1132
  • 10
  • [ 773837-37-9 ]
  • [ 20274-70-8 ]
  • [ 157662-77-6 ]
Reference: [1] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 4, p. 1131 - 1132
  • 11
  • [ 157662-77-6 ]
  • [ 192508-36-4 ]
Reference: [1] Organic Letters, 2002, vol. 4, # 16, p. 2675 - 2678
[2] Tetrahedron, 1999, vol. 55, # 16, p. 5089 - 5112
  • 12
  • [ 67-56-1 ]
  • [ 157662-77-6 ]
  • [ 226888-37-5 ]
Reference: [1] Tetrahedron, 1999, vol. 55, # 16, p. 5089 - 5112
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