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[ CAS No. 115314-14-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 115314-14-2
Chemical Structure| 115314-14-2
Structure of 115314-14-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 115314-14-2 ]

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Product Details of [ 115314-14-2 ]

CAS No. :115314-14-2 MDL No. :MFCD00064582
Formula : C9H9NO6S Boiling Point : No data available
Linear Structure Formula :- InChI Key :AIHIHVZYAAMDPM-QMMMGPOBSA-N
M.W : 259.24 Pubchem ID :146490
Synonyms :

Calculated chemistry of [ 115314-14-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 5
Num. H-bond acceptors : 6.0
Num. H-bond donors : 0.0
Molar Refractivity : 58.03
TPSA : 110.1 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.36 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.74
Log Po/w (XLOGP3) : 0.73
Log Po/w (WLOGP) : 1.78
Log Po/w (MLOGP) : -0.12
Log Po/w (SILICOS-IT) : -0.92
Consensus Log Po/w : 0.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.84
Solubility : 3.76 mg/ml ; 0.0145 mol/l
Class : Very soluble
Log S (Ali) : -2.62
Solubility : 0.621 mg/ml ; 0.00239 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.91
Solubility : 3.17 mg/ml ; 0.0122 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 4.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.49

Safety of [ 115314-14-2 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P210-P201-P264-P280-P370+P378-P308+P313 UN#:1325
Hazard Statements:H315-H319-H341-H228 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 115314-14-2 ]

* 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 [ 115314-14-2 ]

[ 115314-14-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 30818-28-1 ]
  • [ 115314-14-2 ]
  • [ 133715-45-4 ]
  • [ 203259-31-8 ]
  • 2
  • [ 120121-01-9 ]
  • [ 115314-14-2 ]
  • [ 1236375-78-2 ]
  • 3
  • [ 60827-45-4 ]
  • [ 121-51-7 ]
  • [ 115314-14-2 ]
  • 4
  • [ 230301-11-8 ]
  • [ 115314-14-2 ]
  • [ 74-88-4 ]
  • (R)-1-methyl-5-(oxiran-2-ylmethyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine [ No CAS ]
  • (R)-2-methyl-5-(oxiran-2-ylmethyl)-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
To a mixture of 1 -methyl-4,5 ,6,7-tetrahydro- 1 H-pyrazolo [4,3-c]pyridine and 2- methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine (2.8 g, crude) and KF (3.1 g, 53.7 mmol) in THF(200 mL) was added (S)-oxiran-2-ylmethyl 3-nitrobenzenesulfonate (9.2 g, 35.8 mmol) at 20 C. The mixture was stirred at 40 C for 16 h, at which time LCMS showed the completion of the reactions. The mixture was filtered and concentrated to give the crude mixed product (4.9 g, crude), which was used in next step without further purification. LCMS (mlz): 194.2 [M+H]+.
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