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[ CAS No. 496-46-8 ] {[proInfo.proName]}

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Chemical Structure| 496-46-8
Chemical Structure| 496-46-8
Structure of 496-46-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 496-46-8 ]

CAS No. :496-46-8 MDL No. :MFCD00005539
Formula : C4H6N4O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VPVSTMAPERLKKM-UHFFFAOYSA-N
M.W : 142.12 Pubchem ID :62347
Synonyms :

Calculated chemistry of [ 496-46-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 4.0
Molar Refractivity : 45.16
TPSA : 82.26 ?2

Pharmacokinetics

GI absorption : Low
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) : -8.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : -0.29
Log Po/w (XLOGP3) : -1.61
Log Po/w (WLOGP) : -3.26
Log Po/w (MLOGP) : -1.36
Log Po/w (SILICOS-IT) : -1.39
Consensus Log Po/w : -1.58

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.29
Solubility : 279.0 mg/ml ; 1.96 mol/l
Class : Highly soluble
Log S (Ali) : 0.39
Solubility : 350.0 mg/ml ; 2.47 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.48
Solubility : 47.1 mg/ml ; 0.331 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.71

Safety of [ 496-46-8 ]

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

Application In Synthesis of [ 496-46-8 ]

* 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 [ 496-46-8 ]

[ 496-46-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 496-46-8 ]
  • [ 17464-88-9 ]
  • [ 80262-44-8 ]
  • [ 259886-51-6 ]
  • [ 259886-50-5 ]
YieldReaction ConditionsOperation in experiment
Ca. 58%Spectr.; Ca. 9%Spectr.; Ca. 28%Spectr. With methanesulfonic acid; at 80 - 100℃; for 18.0h; Synthesis of cucurbit[n]urils in methanesulphonic acid usingTetramethoxymethylglycoluril (TMMG)Unsubstituted glycoluril (19.94 g) and methane sulphonic acid (neat, 82 ml_) were placed in a reaction flask and heated to 80 °C. TMMG (44.66 g) was added in drop-wise and the reaction mixture was then heated to 100 °C (internal temp) for 18 hours. The reaction mixture was cooled and added to methanol (410 ml) to produce a beige powder which was analysed by1H NMR. Approximate Yields b1H NMR (percent of recovered product) cucurbit[5]uri 5percent, cucurbit[6]uri 58percent, cucurbit[7]uril 28percent, cucurbit[8]uril 9percent, cucurbit[9]uril 0percent, cucurbit[10]uril 0percent, cucurbit[11]uril 0percent
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