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[ CAS No. 57963-11-8 ] {[proInfo.proName]}

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Chemical Structure| 57963-11-8
Chemical Structure| 57963-11-8
Structure of 57963-11-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 57963-11-8 ]

CAS No. :57963-11-8 MDL No. :MFCD09027052
Formula : C7H10N2 Boiling Point : -
Linear Structure Formula :- InChI Key :VYQFIVPHBLAONR-UHFFFAOYSA-N
M.W : 122.17 Pubchem ID :12404013
Synonyms :

Calculated chemistry of [ 57963-11-8 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.57
TPSA : 38.91 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 1.23
Log Po/w (WLOGP) : 1.29
Log Po/w (MLOGP) : 0.89
Log Po/w (SILICOS-IT) : 1.54
Consensus Log Po/w : 1.29

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.87
Solubility : 1.66 mg/ml ; 0.0136 mol/l
Class : Very soluble
Log S (Ali) : -1.64
Solubility : 2.77 mg/ml ; 0.0227 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.39
Solubility : 0.493 mg/ml ; 0.00404 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.41

Safety of [ 57963-11-8 ]

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

Application In Synthesis of [ 57963-11-8 ]

* 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 [ 57963-11-8 ]
  • Downstream synthetic route of [ 57963-11-8 ]

[ 57963-11-8 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 1233520-02-9 ]
  • [ 57963-11-8 ]
Reference: [1] Patent: WO2010/72722, 2010, A1, . Location in patent: Page/Page column 33
  • 2
  • [ 100-54-9 ]
  • [ 100-48-1 ]
  • [ 79-06-1 ]
  • [ 57963-11-8 ]
Reference: [1] Patent: US4672121, 1987, A,
  • 3
  • [ 583-58-4 ]
  • [ 57963-11-8 ]
  • [ 823-39-2 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1981, vol. 18, p. 1613 - 1618
[2] Journal of Heterocyclic Chemistry, 2008, vol. 45, # 3, p. 661 - 665
  • 4
  • [ 1796-86-7 ]
  • [ 57963-11-8 ]
Reference: [1] Bioorganic and medicinal chemistry letters, 2000, vol. 10, # 17, p. 1975 - 1978
[2] Patent: WO2008/141119, 2008, A2,
  • 5
  • [ 583-58-4 ]
  • [ 121-69-7 ]
  • [ 57963-11-8 ]
  • [ 823-39-2 ]
Reference: [1] Patent: US5972975, 1999, A,
  • 6
  • [ 583-58-4 ]
  • [ 57963-11-8 ]
Reference: [1] Patent: WO2008/141119, 2008, A2,
  • 7
  • [ 583-58-4 ]
  • [ 57963-11-8 ]
  • [ 823-39-2 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1981, vol. 18, p. 1613 - 1618
[2] Journal of Heterocyclic Chemistry, 2008, vol. 45, # 3, p. 661 - 665
  • 8
  • [ 583-58-4 ]
  • [ 121-69-7 ]
  • [ 57963-11-8 ]
  • [ 823-39-2 ]
Reference: [1] Patent: US5972975, 1999, A,
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