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[ CAS No. 4887-80-3 ] {[proInfo.proName]}

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Chemical Structure| 4887-80-3
Chemical Structure| 4887-80-3
Structure of 4887-80-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4887-80-3 ]

CAS No. :4887-80-3 MDL No. :MFCD00272526
Formula : C8H8N2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :ILMHAGCURJPNRZ-UHFFFAOYSA-N
M.W : 148.16 Pubchem ID :78598
Synonyms :

Calculated chemistry of [ 4887-80-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.59
TPSA : 37.91 ?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) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.25
Log Po/w (XLOGP3) : 1.78
Log Po/w (WLOGP) : 1.57
Log Po/w (MLOGP) : 0.7
Log Po/w (SILICOS-IT) : 2.02
Consensus Log Po/w : 1.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.42
Solubility : 0.564 mg/ml ; 0.00381 mol/l
Class : Soluble
Log S (Ali) : -2.19
Solubility : 0.947 mg/ml ; 0.00639 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.02
Solubility : 0.142 mg/ml ; 0.000959 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.33

Safety of [ 4887-80-3 ]

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

Application In Synthesis of [ 4887-80-3 ]

* 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 [ 4887-80-3 ]

[ 4887-80-3 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 4887-80-3 ]
  • [ 41292-65-3 ]
YieldReaction ConditionsOperation in experiment
96% for 2 h; Heating / reflux Example 92; 4-(lH-Benzoimidazol-5-yloxy)-N-(4-bromo-phenyl)-3-(7-isopropyl-pyrido[2,3-d]pyrimidin-4- ylamino)-benzamide; Example 92A; lH-Benzoimidazol-5-ol; [0458] A solution of 5-methoxybenzimidazole (500 mg, 3.374 mmol) in 48percent hydrobromic acid (10 mL) was refluxed for 2 hours. The reaction was cooled to room temperature, the solvent removed by rotary evaporation under vacuum, and the residue azeotroped with toluene (50 mL) to provide the title compound as a tan solid (701 mg, 96percent).
Reference: [1] Patent: WO2007/76034, 2007, A2, . Location in patent: Page/Page column 125
[2] Journal of the American Chemical Society, 1955, vol. 77, p. 5192
[3] Synthetic Communications, 2010, vol. 40, # 12, p. 1765 - 1771
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 7, p. 2620 - 2623
  • 2
  • [ 4887-80-3 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry of Natural Compounds, 1983, vol. 19, # 1, p. 124 - 125[2] Khimiya Prirodnykh Soedinenii, 1983, # 1, p. 121
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