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[ CAS No. 14001-60-6 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 14001-60-6
Chemical Structure| 14001-60-6
Chemical Structure| 14001-60-6
Structure of 14001-60-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 14001-60-6 ]

CAS No. :14001-60-6 MDL No. :MFCD03425593
Formula : C6H8N2O Boiling Point : -
Linear Structure Formula :- InChI Key :CDKZAIGAEMFLEO-UHFFFAOYSA-N
M.W : 124.14 Pubchem ID :5063810
Synonyms :

Calculated chemistry of [ 14001-60-6 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 33.49
TPSA : 35.01 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) : -6.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 0.91
Log Po/w (WLOGP) : 0.79
Log Po/w (MLOGP) : 0.06
Log Po/w (SILICOS-IT) : 1.32
Consensus Log Po/w : 0.98

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.61
Solubility : 3.05 mg/ml ; 0.0245 mol/l
Class : Very soluble
Log S (Ali) : -1.23
Solubility : 7.3 mg/ml ; 0.0588 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.12
Solubility : 0.935 mg/ml ; 0.00753 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.68

Safety of [ 14001-60-6 ]

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

Application In Synthesis of [ 14001-60-6 ]

* 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 [ 14001-60-6 ]
  • Downstream synthetic route of [ 14001-60-6 ]

[ 14001-60-6 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 67-56-1 ]
  • [ 5348-51-6 ]
  • [ 14001-60-6 ]
Reference: [1] Organic Letters, 2010, vol. 12, # 20, p. 4478 - 4481
  • 2
  • [ 56681-97-1 ]
  • [ 2440-60-0 ]
  • [ 14001-60-6 ]
Reference: [1] Patent: WO2009/101078, 2009, A1, . Location in patent: Page/Page column 76
  • 3
  • [ 5424-21-5 ]
  • [ 14001-60-6 ]
Reference: [1] Journal of the Chemical Society, 1951, p. 1004,1015[2] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, vol. 24, p. 84
  • 4
  • [ 13036-57-2 ]
  • [ 4637-24-5 ]
  • [ 14001-60-6 ]
  • [ 99357-40-1 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1996, vol. 33, # 2, p. 465 - 474
  • 5
  • [ 13036-57-2 ]
  • [ 124-41-4 ]
  • [ 14001-60-6 ]
Reference: [1] Yakugaku Zasshi, 1942, vol. 62, p. 315,333; dtsch. Ref. S. 95, 106[2] Chem.Abstr., 1951, p. 5150
[3] Journal of the Chemical Society, 1951, p. 1004,1015[4] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, vol. 24, p. 84
  • 6
  • [ 14001-60-6 ]
  • [ 944901-04-6 ]
Reference: [1] Patent: WO2009/101078, 2009, A1,
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