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[ CAS No. 6304-16-1 ] {[proInfo.proName]}

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Chemical Structure| 6304-16-1
Chemical Structure| 6304-16-1
Structure of 6304-16-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6304-16-1 ]

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Product Details of [ 6304-16-1 ]

CAS No. :6304-16-1 MDL No. :MFCD00129043
Formula : C8H9NO Boiling Point : -
Linear Structure Formula :- InChI Key :ILRVKOYYFFNXDB-UHFFFAOYSA-N
M.W : 135.16 Pubchem ID :80552
Synonyms :

Calculated chemistry of [ 6304-16-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.02
TPSA : 29.96 ?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) : -6.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.41
Log Po/w (XLOGP3) : 0.47
Log Po/w (WLOGP) : 1.21
Log Po/w (MLOGP) : 0.46
Log Po/w (SILICOS-IT) : 1.98
Consensus Log Po/w : 1.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.29
Solubility : 6.99 mg/ml ; 0.0517 mol/l
Class : Very soluble
Log S (Ali) : -0.67
Solubility : 29.0 mg/ml ; 0.215 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.25 mg/ml ; 0.00185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.11

Safety of [ 6304-16-1 ]

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

Application In Synthesis of [ 6304-16-1 ]

* 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 [ 6304-16-1 ]

[ 6304-16-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 6304-16-1 ]
  • [ 123-06-8 ]
  • [ 78415-72-2 ]
YieldReaction ConditionsOperation in experiment
In ethanol; EXAMPLE 1 A mixture containing 13.5 g. of 4-pyridinylmethyl methyl ketone, 12.2 g. of ethoxymethylenemalononitrile and 100 ml. of ethanol was refluxed with stirring for five hours and then allowed to cool to room temperature. The separated crystalline product was collected, washed with cold ethanol and dried in a vacuum oven at 60 C. to yield 14.2 g. of 1,2-dihydro-6-methyl-2-oxo-5-(4-pyridinyl)nicotinonitrile, m.p. >300 C. The nuclear magnetic resonance and infrared spectra of this product were identical with the corresponding respective spectra of the same compound prepared by a different method, that is, by reacting 1-(4-pyridinyl)-2-(dimethylamino)ethenyl methyl ketone with alpha-cyanoacetamide.
  • 3
  • [ 6304-16-1 ]
  • [ 80047-24-1 ]
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