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[ CAS No. 2080-75-3 ] {[proInfo.proName]}

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Chemical Structure| 2080-75-3
Chemical Structure| 2080-75-3
Structure of 2080-75-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2080-75-3 ]

CAS No. :2080-75-3 MDL No. :MFCD01462048
Formula : C8H8N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AUPLVAKFTYFHTA-UHFFFAOYSA-N
M.W : 164.16 Pubchem ID :591101
Synonyms :
Chemical Name :5-Methoxy-1H-benzo[d]imidazol-2(3H)-one

Calculated chemistry of [ 2080-75-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 45.41
TPSA : 57.88 ?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) : -6.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.42
Log Po/w (XLOGP3) : 0.53
Log Po/w (WLOGP) : 0.86
Log Po/w (MLOGP) : 0.58
Log Po/w (SILICOS-IT) : 2.13
Consensus Log Po/w : 1.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.68
Solubility : 3.42 mg/ml ; 0.0209 mol/l
Class : Very soluble
Log S (Ali) : -1.32
Solubility : 7.92 mg/ml ; 0.0482 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.94
Solubility : 0.19 mg/ml ; 0.00116 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.45

Safety of [ 2080-75-3 ]

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

Application In Synthesis of [ 2080-75-3 ]

* 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 [ 2080-75-3 ]

[ 2080-75-3 ] Synthesis Path-Upstream   1~15

  • 1
  • [ 213118-56-0 ]
  • [ 2080-75-3 ]
YieldReaction ConditionsOperation in experiment
72% With potassium carbonate In N,N-dimethyl-formamide at 130℃; for 5 h; Intermediate 37:[0168] Intermediate 36 (7.3 g, 30.6 mmol) was dissolved in DMF (70 mL). To this solution was added anhydrous K2C03 (4.7 g, 33.7 mmol) and the mixture was heated to reflux (130°C) for 5 h. The solvent was removed under pressure, the residue was poured into ice water, and the aq phase was extracted with EtOAc. The combined organic layers were dried over anhydrous Na2S04, concentrated under vacuum, and the resulting yellow solid was recrystallized from EtOH to give 5-methoxy-lH-benzo[^imidazol-2(3H)-one (intermediate 37) (3.6 g, 72percent) as a yellow solid, mp: 249-251°C.
Reference: [1] Patent: WO2012/3418, 2012, A2, . Location in patent: Page/Page column 71
  • 2
  • [ 32315-10-9 ]
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2016, vol. 7, # 6, p. 552 - 557
  • 3
  • [ 623-49-4 ]
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] Letters in Organic Chemistry, 2011, vol. 8, # 6, p. 406 - 411
  • 4
  • [ 96-96-8 ]
  • [ 2080-75-3 ]
Reference: [1] European Journal of Organic Chemistry, 2019,
  • 5
  • [ 124-38-9 ]
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry - An Asian Journal, 2016, vol. 11, # 19, p. 2735 - 2740
  • 6
  • [ 57-13-6 ]
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] MedChemComm, 2013, vol. 4, # 3, p. 527 - 529
  • 7
  • [ 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
  • 8
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] Patent: WO2012/3418, 2012, A2,
[2] Letters in Organic Chemistry, 2011, vol. 8, # 6, p. 406 - 411
  • 9
  • [ 96-96-8 ]
  • [ 2080-75-3 ]
Reference: [1] Patent: WO2012/3418, 2012, A2,
  • 10
  • [ 1329028-11-6 ]
  • [ 2080-75-3 ]
Reference: [1] Letters in Organic Chemistry, 2011, vol. 8, # 6, p. 406 - 411
  • 11
  • [ 27185-61-1 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry - A European Journal, 2014, vol. 20, # 43, p. 13854 - 13859
  • 12
  • [ 104-94-9 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry - A European Journal, 2014, vol. 20, # 43, p. 13854 - 13859
  • 13
  • [ 1150-26-1 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry - A European Journal, 2014, vol. 20, # 43, p. 13854 - 13859
  • 14
  • [ 3360-81-4 ]
  • [ 2080-75-3 ]
Reference: [1] Chemistry - A European Journal, 2014, vol. 20, # 43, p. 13854 - 13859
  • 15
  • [ 530-62-1 ]
  • [ 102-51-2 ]
  • [ 2080-75-3 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 3, p. 719 - 723
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