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[ CAS No. 4425-56-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4425-56-3
Chemical Structure| 4425-56-3
Structure of 4425-56-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4425-56-3 ]

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Product Details of [ 4425-56-3 ]

CAS No. :4425-56-3 MDL No. :MFCD00051958
Formula : C5H3N3O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HAUXRJCZDHHADG-UHFFFAOYSA-N
M.W : 137.10 Pubchem ID :78145
Synonyms :

Calculated chemistry of [ 4425-56-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 32.4
TPSA : 89.51 ?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) : -7.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.12
Log Po/w (XLOGP3) : -0.93
Log Po/w (WLOGP) : -1.07
Log Po/w (MLOGP) : -1.71
Log Po/w (SILICOS-IT) : 1.2
Consensus Log Po/w : -0.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.55
Solubility : 38.8 mg/ml ; 0.283 mol/l
Class : Very soluble
Log S (Ali) : -0.47
Solubility : 46.9 mg/ml ; 0.342 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.52
Solubility : 4.11 mg/ml ; 0.03 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.69

Safety of [ 4425-56-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4425-56-3 ]

* 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 [ 4425-56-3 ]

[ 4425-56-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4425-56-3 ]
  • [ 23945-44-0 ]
  • 2
  • [ 4425-56-3 ]
  • [ 3177-24-0 ]
YieldReaction ConditionsOperation in experiment
With N,N-diethylaniline; trichlorophosphate; at 25 - 115℃; for 3h; To a mixture of the above uracil (15.41 g, 112.5 mmol) and phosphorus oxychloride (157.4 mL, 1.69 mol) was added N,N-diethylaniline (34.2 mL, 225 mmol), cautiously, at 25 C. The reaction was then heated at 115 C. for 3 h after which the mixture was cooled to 40 C. and concentrated in vacuo to remove excess POCl3. The remaining liquid was poured slowly onto ice-water with rapid stirring and the precipitated product was filtered. The aqueous layer was then extracted with chloroform and the extract was washed with 1 N HCl before concentrating in vacuo. This material was combined with the previously filtered material to afford 2,4-dichloro-pyrimidine-5-carbonitrile (15.36 g, 79%).
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