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[ CAS No. 30414-55-2 ] {[proInfo.proName]}

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Chemical Structure| 30414-55-2
Chemical Structure| 30414-55-2
Structure of 30414-55-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 30414-55-2 ]

CAS No. :30414-55-2 MDL No. :MFCD12031307
Formula : C8H14O3 Boiling Point : -
Linear Structure Formula :- InChI Key :WUGKTJAKSVEAFG-UHFFFAOYSA-N
M.W : 158.20 Pubchem ID :121701
Synonyms :

Calculated chemistry of [ 30414-55-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.05
TPSA : 43.37 ?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) : -6.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 1.23
Log Po/w (WLOGP) : 1.16
Log Po/w (MLOGP) : 0.97
Log Po/w (SILICOS-IT) : 1.38
Consensus Log Po/w : 1.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.27
Solubility : 8.58 mg/ml ; 0.0542 mol/l
Class : Very soluble
Log S (Ali) : -1.74
Solubility : 2.89 mg/ml ; 0.0183 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.52
Solubility : 4.72 mg/ml ; 0.0299 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 30414-55-2 ]

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

Application In Synthesis of [ 30414-55-2 ]

* 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 [ 30414-55-2 ]

[ 30414-55-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 30414-55-2 ]
  • [ 57297-29-7 ]
  • [ 945955-11-3 ]
YieldReaction ConditionsOperation in experiment
7.5% Reference Example 10; 2-cyclopropyl-4 -isobutyl-6-methoxypyrimidine-5- carbaldehyde; (step 1); To a solution of methyl 5-methyl-3-oxohexanoate(14.3 g) synthesized by a known method (WO2006/090915) and cyclopropylcarbamidine monohydrochloride (10.9 g) in ethanol (180 mL) was added sodium ethoxide (18.5 g) at room temperature, and the mixture was heated under reflux for 4 hrs. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in water and acidified with 6N hydrochloric acid at 0°C. The resultant product was extracted 3 times with ethyl acetate, and the organic layer was washed with brine.' The organic layer was dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 50-67percent ethyl acetate/hexane) and crystallized from ethyl acetate-IPE to give 2-cyclopropyl-6-isobutylpyrimidine- 4-ol (1.31 g, 7.5percent) as. a white powder.1H-NMR (300MHz, CDCl3): deltapsi.91 (6H, d, J=6.4Hz), 1.03- 1.12 (2H, m) , 1.14-1.22 (2H, m) , 1.86-1.95 (IH, m) , 1.99-2.10 (IH, m) , 2.31 (2H, d, J=7.2Hz), 6.05 (IH, s), 13.38 (IH, br)
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