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[ CAS No. 108-26-9 ] {[proInfo.proName]}

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Chemical Structure| 108-26-9
Chemical Structure| 108-26-9
Structure of 108-26-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 108-26-9 ]

CAS No. :108-26-9 MDL No. :MFCD00020699
Formula : C4H6N2O Boiling Point : No data available
Linear Structure Formula :C3H3N2(CH3)(O) InChI Key :NHLAPJMCARJFOG-UHFFFAOYSA-N
M.W : 98.10 Pubchem ID :7920
Synonyms :

Calculated chemistry of [ 108-26-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.16
TPSA : 41.46 ?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) : -7.23 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.94
Log Po/w (XLOGP3) : -0.47
Log Po/w (WLOGP) : -0.88
Log Po/w (MLOGP) : -0.49
Log Po/w (SILICOS-IT) : 1.27
Consensus Log Po/w : 0.08

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.15
Solubility : 69.1 mg/ml ; 0.704 mol/l
Class : Very soluble
Log S (Ali) : 0.07
Solubility : 114.0 mg/ml ; 1.16 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.99
Solubility : 10.1 mg/ml ; 0.103 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.46

Safety of [ 108-26-9 ]

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

Application In Synthesis of [ 108-26-9 ]

* 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 [ 108-26-9 ]

[ 108-26-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 108-24-7 ]
  • [ 122-51-0 ]
  • [ 108-26-9 ]
  • [ 13214-64-7 ]
  • <i>N</i>-(1-acetyl-3-methyl-6-oxo-1,6-dihydro-pyrano[2,3-<i>c</i>]pyrazol-5-yl)-4-methoxy-benzamide [ No CAS ]
  • 2
  • [ 399-25-7 ]
  • [ 108-26-9 ]
  • C12H12FN3O3 [ No CAS ]
  • C12H12FN3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With C33H30F6N4O3; In dichloromethane; at 20℃; for 24h;Inert atmosphere; General procedure: To a solution of nitroolefin 3 (0.33 mmol) in CH2Cl2 (1.5 ml) was added bifunctional catalyst 1i (2 mg,0.0033 mmol, 1 mol %) and the mixture was stirred for 5 min under N2 atmosphere. Then pyrazolin-5-one 2 (0.4 mmol) was added to the mixture. Upon consumption of nitroolefin substrate (monitored by TLC), the reaction mixture was concentrated and purified by silica gel column chromatography to afford the conjugate addition products 4.
  • 3
  • [ 2737-22-6 ]
  • [ 108-26-9 ]
  • C11H7Br3N2O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic acid; In dimethyl sulfoxide; at 55℃; for 3h;Microwave irradiation; General procedure: All reactions were carried out in PCR tubes at 50 μL scale. The reactantswere dissolved in DMSO to a final concentration of 40 mM (1.0equiv), and 0.3 μL glacial acetic acid (2.0 equiv) was added as a catalyst.The reaction mixtures were heated in a real-time PCR detection systems(Bio-Rad, CFX96) at 55 for 3 h,followed by cooing to roomtemperature.
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