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[ CAS No. 5391-39-9 ] {[proInfo.proName]}

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Chemical Structure| 5391-39-9
Chemical Structure| 5391-39-9
Structure of 5391-39-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5391-39-9 ]

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Product Details of [ 5391-39-9 ]

CAS No. :5391-39-9 MDL No. :MFCD00988254
Formula : C5H8N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :JJWACYUTERPMBM-UHFFFAOYSA-N
M.W : 128.13 Pubchem ID :79350
Synonyms :
Chemical Name :1-Acetylimidazolidin-2-one

Calculated chemistry of [ 5391-39-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.6
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.35
TPSA : 49.41 ?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) : -7.71 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.48
Log Po/w (XLOGP3) : -0.89
Log Po/w (WLOGP) : -1.2
Log Po/w (MLOGP) : -0.52
Log Po/w (SILICOS-IT) : -0.2
Consensus Log Po/w : -0.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.01
Solubility : 126.0 mg/ml ; 0.982 mol/l
Class : Very soluble
Log S (Ali) : 0.33
Solubility : 277.0 mg/ml ; 2.16 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.28
Solubility : 66.6 mg/ml ; 0.52 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.32

Safety of [ 5391-39-9 ]

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

Application In Synthesis of [ 5391-39-9 ]

* 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 [ 5391-39-9 ]

[ 5391-39-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5391-39-9 ]
  • [ 32202-61-2 ]
  • [ 67356-94-9 ]
  • 2
  • [ 5391-39-9 ]
  • [ 1075-35-0 ]
  • 5-chloro-2-methyl-3-(4,5-dihydro-1-H-imidazol-2-yl)-1H-indole [ No CAS ]
YieldReaction ConditionsOperation in experiment
26% With trichlorophosphate; In ethanol; at 50℃; for 8.5h;Heating / reflux; A mixture of <strong>[1075-35-0]5-chloro-2-methylindole</strong> (30.1 g; 0.18 mole) and 1-acetyl-imidazolidine-2-one (24 g; 0.18 mole) was added to phosphorous oxychloride (178 ml) and heated to 50 C. After 5 hours, phosphorous oxychloride was evaporated. The residue was treated with ethanol (250 ml) cautiously and maintained at reflux for 3.5 hours. The mixture was concentrated under reduced pressure to half of the orignal volume to obtain a precipitate, which was collected on a filter. The crystalline residue was treated with water, washed with ethylacetate, treated with 2N sodium hydroxide to pH 11 and stirred overnight. The precipitate was filtered, washed with water and t-butylmethylether and dried to give product (10.9 g, 26%), m.p. 213 C. [0467] 1H-NMR(DMSO): d 2.5 (s, 3H, CH-31), 3.55 (s, 4H, 2×CH-2), 6.30 (b, 1H, imidazolin), 7.04 (d, 1H 8.00 (s, 1H, H-4), 11.57 (b, 1H, NH-indol); MS (Ei 70 eV) m/Z 233M+.
  • 4
  • [ 5391-39-9 ]
  • [ 1075-34-9 ]
  • 5-bromo-3-(4,5-dihydro-1H-imidazol-2-yl)-2-methyl-1H-indole hydrochloride [ No CAS ]
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