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[ CAS No. 105125-43-7 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 105125-43-7
Chemical Structure| 105125-43-7
Chemical Structure| 105125-43-7
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Product Details of [ 105125-43-7 ]

CAS No. :105125-43-7 MDL No. :MFCD27991313
Formula : C10H8N2O3S Boiling Point : -
Linear Structure Formula :- InChI Key :YIZMNGKCMZDQJW-UHFFFAOYSA-N
M.W : 236.25 Pubchem ID :13613762
Synonyms :

Calculated chemistry of [ 105125-43-7 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 4
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 58.01
TPSA : 80.52 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 1.84
Log Po/w (WLOGP) : 2.38
Log Po/w (MLOGP) : 0.43
Log Po/w (SILICOS-IT) : 0.26
Consensus Log Po/w : 1.37

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.75
Solubility : 0.415 mg/ml ; 0.00176 mol/l
Class : Soluble
Log S (Ali) : -3.15
Solubility : 0.167 mg/ml ; 0.000706 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.67
Solubility : 0.0499 mg/ml ; 0.000211 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.12

Safety of [ 105125-43-7 ]

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 [ 105125-43-7 ]

* 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 [ 105125-43-7 ]
  • Downstream synthetic route of [ 105125-43-7 ]

[ 105125-43-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 142-08-5 ]
  • [ 105125-43-7 ]
YieldReaction ConditionsOperation in experiment
91% With thionyl chloride; triethylamine In tetrahydrofuran (128-2)
Under nitrogen atmosphere, to a solution of 2-hydroxypyridine (2.66 g) and NEt3 (4.05 mL) in THF (80 mL) was added dropwise SOCl2 (1.05 mL) under ice-cooling, and the mixture was stirred for one hour.
The mixture was filtered, and the solvent was evaporated under reduced pressure to give di-2-pyridyl sulfite (3.02 g, 91percent).
91% With thionyl chloride; triethylamine In tetrahydrofuran (128-2)
Under nitrogen atmosphere, to a solution of 2-hydroxypyridine (2.66 g) and NEt3 (4.05 mL) in THF (80 mL) was added dropwise SOCl2 (1.05 mL) under ice-cooling, and the mixture was stirred for one hour.
The mixture was filtered, and the solvent was evaporated under reduced pressure to give di-2-pyridyl sulfite (3.02 g, 91 percent).
Reference: [1] Patent: US2003/181496, 2003, A1,
[2] Patent: EP1479384, 2004, A1,
[3] Tetrahedron Letters, 1986, vol. 27, # 17, p. 1925 - 1928
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