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[ CAS No. 1483-31-4 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1483-31-4
Chemical Structure| 1483-31-4
Chemical Structure| 1483-31-4
Structure of 1483-31-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1483-31-4 ]

CAS No. :1483-31-4 MDL No. :MFCD00598097
Formula : C8H5ClN2O Boiling Point : -
Linear Structure Formula :- InChI Key :QSGNNXKJPIMRPO-UHFFFAOYSA-N
M.W : 180.59 Pubchem ID :12267312
Synonyms :

Calculated chemistry of [ 1483-31-4 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.74
TPSA : 38.92 Ų

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) : -5.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.27
Log Po/w (XLOGP3) : 2.94
Log Po/w (WLOGP) : 2.39
Log Po/w (MLOGP) : 1.93
Log Po/w (SILICOS-IT) : 2.58
Consensus Log Po/w : 2.42

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.42
Solubility : 0.068 mg/ml ; 0.000377 mol/l
Class : Soluble
Log S (Ali) : -3.42
Solubility : 0.0688 mg/ml ; 0.000381 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.0
Solubility : 0.0181 mg/ml ; 0.0001 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.04

Safety of [ 1483-31-4 ]

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

Application In Synthesis of [ 1483-31-4 ]

* 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 [ 1483-31-4 ]
  • Downstream synthetic route of [ 1483-31-4 ]

[ 1483-31-4 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 1612-76-6 ]
  • [ 1483-31-4 ]
Reference: [1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 9, p. 3543 - 3550
  • 2
  • [ 1199-02-6 ]
  • [ 1483-31-4 ]
Reference: [1] Acta Chimica Academiae Scientiarum Hungaricae, 1982, vol. 110, # 2, p. 133 - 144
[2] Journal of the Indian Chemical Society, 1984, vol. 61, # 5, p. 436 - 439
[3] Journal of Heterocyclic Chemistry, 1973, vol. 10, p. 989 - 991
  • 3
  • [ 825-56-9 ]
  • [ 1483-31-4 ]
Reference: [1] European Journal of Organic Chemistry, 2015, vol. 2015, # 1, p. 77 - 80
  • 4
  • [ 614-22-2 ]
  • [ 1483-31-4 ]
Reference: [1] Journal of the Indian Chemical Society, 1984, vol. 61, # 5, p. 436 - 439
[2] Acta Chimica Academiae Scientiarum Hungaricae, 1982, vol. 110, # 2, p. 133 - 144
  • 5
  • [ 613-94-5 ]
  • [ 1483-31-4 ]
Reference: [1] European Journal of Organic Chemistry, 2015, vol. 2015, # 1, p. 77 - 80
  • 6
  • [ 65-85-0 ]
  • [ 1483-31-4 ]
Reference: [1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 9, p. 3543 - 3550
  • 7
  • [ 57943-70-1 ]
  • [ 3294-58-4 ]
  • [ 1483-31-4 ]
Reference: [1] Journal of Organic Chemistry, 1974, vol. 39, p. 2336 - 2341
  • 8
  • [ 10465-97-1 ]
  • [ 1483-31-4 ]
Reference: [1] Indian Journal of Chemistry, 1969, vol. 7, p. 760 - 765
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