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[ CAS No. 67383-32-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 67383-32-8
Chemical Structure| 67383-32-8
Structure of 67383-32-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 67383-32-8 ]

CAS No. :67383-32-8 MDL No. :MFCD00223606
Formula : C8H10N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :KTZQDIINDVWLES-UHFFFAOYSA-N
M.W : 182.18 Pubchem ID :293750
Synonyms :

Calculated chemistry of [ 67383-32-8 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.38
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 45.91
TPSA : 72.05 Ų

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) : -7.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.47
Log Po/w (XLOGP3) : -0.3
Log Po/w (WLOGP) : 0.26
Log Po/w (MLOGP) : 0.11
Log Po/w (SILICOS-IT) : 1.64
Consensus Log Po/w : 0.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.92
Solubility : 21.7 mg/ml ; 0.119 mol/l
Class : Very soluble
Log S (Ali) : -0.75
Solubility : 32.2 mg/ml ; 0.177 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.43
Solubility : 0.68 mg/ml ; 0.00373 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.92

Safety of [ 67383-32-8 ]

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

Application In Synthesis of [ 67383-32-8 ]

* 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 [ 67383-32-8 ]

[ 67383-32-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67383-32-8 ]
  • [ 5469-26-1 ]
  • [ 335278-70-1 ]
YieldReaction ConditionsOperation in experiment
With tetrabutyl ammonium fluoride; In 1,2-dimethoxyethane; Step 2A 5-Ethoxycarbonyl-2-methyl-3-(2-oxo-3,3-dimethyl-butyl)pyrimid-4-one To a suspension of <strong>[67383-32-8]5-ethoxycarbonyl-2-methylpyrimid-4-one</strong> (2.7 g, 14.75 mmol.) in DME (20 ml), tetrabutylammonium fluoride (22 ml, 22.0 mmol.) was added. The solution was stirred at room temperature until solids dissolved, then 1-bromopinacolone (2.2 ml, 1.1 eq., 16.22 mmol) was added. The solution was stirred overnight and concentrated to a brown oil. The crude mixture was purified by silica gel column chromatography (hexane/ethyl acetate, 100/0 to 0/100). A less polar O-alkylated by-product was eluted first (1.8 g) and then the desired N-alkylated product (1.1 g); MS (281, M+H)+. NMR (CDCl3, delta): 8.57 (1H, s), 5.06(1H, s), 4.35(2H, q), 2.42 (3H, s), 1.34 (3H, t), 1.30 (9H,s).
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