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[ CAS No. 105596-63-2 ] {[proInfo.proName]}

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Chemical Structure| 105596-63-2
Chemical Structure| 105596-63-2
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Product Details of [ 105596-63-2 ]

CAS No. :105596-63-2 MDL No. :MFCD04115718
Formula : C7H7NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :DPNDWFVORIGXQO-UHFFFAOYSA-N
M.W : 153.14 Pubchem ID :819942
Synonyms :

Calculated chemistry of [ 105596-63-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 37.69
TPSA : 59.42 ?2

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) : -6.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.3
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : 0.79
Log Po/w (MLOGP) : -0.96
Log Po/w (SILICOS-IT) : 0.71
Consensus Log Po/w : 0.55

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.63
Solubility : 3.61 mg/ml ; 0.0235 mol/l
Class : Very soluble
Log S (Ali) : -1.73
Solubility : 2.83 mg/ml ; 0.0185 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.51
Solubility : 4.73 mg/ml ; 0.0309 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 105596-63-2 ]

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

Application In Synthesis of [ 105596-63-2 ]

* 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.

  • Downstream synthetic route of [ 105596-63-2 ]

[ 105596-63-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15855-06-8 ]
  • [ 105596-63-2 ]
YieldReaction ConditionsOperation in experiment
78% With hydrogen; triethylamine;palladium 10% on activated carbon; In methanol; at 20℃; under 155.149 Torr; To a suspension of the title compound of Preparation 22 (1.94 g, 6.49 mmol) in acetonitrile (150 mL), sodium iodide (4.90 g, 32.69 mmol) and trimethylsilyl chloride (4.10 mL, 32.42 mmol) were added. The resulting suspension was stirred under nitrogen atmosphere at 400C for 3 days. The mixture was cooled to O0C and the solid was filtered off, washed with acetonitrile and dried to yield 1.66 g (90%) of the title compound.LRMS: m/z 285(M+1 )+ Retention time: 2.86min (method B)
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