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[ CAS No. 1128-61-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1128-61-6
Chemical Structure| 1128-61-6
Structure of 1128-61-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1128-61-6 ]

CAS No. :1128-61-6 MDL No. :MFCD00041233
Formula : C10H8FN Boiling Point : No data available
Linear Structure Formula :- InChI Key :GPIARMSVZOEZCV-UHFFFAOYSA-N
M.W : 161.18 Pubchem ID :70784
Synonyms :

Calculated chemistry of [ 1128-61-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.1
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.67
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) : -5.37 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.14
Log Po/w (XLOGP3) : 2.69
Log Po/w (WLOGP) : 3.1
Log Po/w (MLOGP) : 2.56
Log Po/w (SILICOS-IT) : 3.34
Consensus Log Po/w : 2.77

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.15
Solubility : 0.114 mg/ml ; 0.000707 mol/l
Class : Soluble
Log S (Ali) : -2.61
Solubility : 0.393 mg/ml ; 0.00244 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.36
Solubility : 0.0071 mg/ml ; 0.0000441 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.26

Safety of [ 1128-61-6 ]

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

Application In Synthesis of [ 1128-61-6 ]

* 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.

  • Downstream synthetic route of [ 1128-61-6 ]

[ 1128-61-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1128-61-6 ]
  • [ 92-55-7 ]
  • (E)-6-fluoro-2-[2-(5-nitrofuran-2-yl)vinyl]quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With acetic anhydride; at 150℃; for 30h; General procedure: A mixture of 2-methylquinoline (5a, 0.14 g, 1 mmol), <strong>[92-55-7](5-nitrofuran-2-yl)methylene diacetate</strong> (0.72 g, 3 mmol) and acetic anhydride (30 mL) was heated at 150 C for 30 h (TLC monitoring). After cooling, the solvent was removed in vacuo to provide the crude product, which was purified by flash column chromatography (FC, silica gel use CH2Cl2 as eluent) to give 6a (0.22 g, 81%) as a yellow solid.
  • 3
  • [ 1128-61-6 ]
  • [ 5780-66-5 ]
  • C15H10FN3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
68% With toluene-4-sulfonamide; In toluene; at 120℃; for 12h;Inert atmosphere; A solution of 6-fluoro-2-methylquinoline (200 mg, 1.24 mmol), p-toluenesulfonamide (212 mg, 1.24 mmol) and pyrazine-2-carbaldehyde (134 mg, 1.24 mmol) in toluene (4 mL) was refluxed at 120° C. for 12 h in a reaction tube under N2. After the mixture was cooled to room temperature, the solvent was removed under reduced pressure. Then the concentrate was purified by column chromatography with EtOAc/Hexane (1:4, v/v) on silica gel, affording TZ-36-22 as a light yellow solid (211 mg, 68percent). 1H NMR (400 MHz, DMSO-d6) delta 8.93 (d, J=1.4 Hz, 1H), 8.67 (dd, J=2.4, 1.5 Hz, 1H), 8.55 (d, J=2.5 Hz, 1H), 8.38 (d, J=8.6 Hz, 1H), 8.07 (dd, J=9.3, 5.5 Hz, 1H), 7.93 (dd, J=15.5, 6.2 Hz, 3H), 7.77 (dd, J=9.4, 2.9 Hz, 1H), 7.66 (td, J=8.9, 2.9 Hz, 1H).
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