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[ CAS No. 3484-35-3 ] {[proInfo.proName]}

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Chemical Structure| 3484-35-3
Chemical Structure| 3484-35-3
Structure of 3484-35-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3484-35-3 ]

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Product Details of [ 3484-35-3 ]

CAS No. :3484-35-3 MDL No. :MFCD02379906
Formula : C9H9NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :HXQDSHSATAEREW-UHFFFAOYSA-N
M.W : 147.17 Pubchem ID :5325716
Synonyms :

Calculated chemistry of [ 3484-35-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.7
TPSA : 29.1 ?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) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 1.52
Log Po/w (WLOGP) : 0.92
Log Po/w (MLOGP) : 1.45
Log Po/w (SILICOS-IT) : 2.33
Consensus Log Po/w : 1.57

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.11
Solubility : 1.13 mg/ml ; 0.0077 mol/l
Class : Soluble
Log S (Ali) : -1.74
Solubility : 2.68 mg/ml ; 0.0182 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.25
Solubility : 0.0818 mg/ml ; 0.000556 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.35

Safety of [ 3484-35-3 ]

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

Application In Synthesis of [ 3484-35-3 ]

* 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 [ 3484-35-3 ]

[ 3484-35-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3240-35-5 ]
  • [ 3484-35-3 ]
  • [ 1261152-99-1 ]
  • 2
  • [ 3484-35-3 ]
  • [ 3012-80-4 ]
  • (E)-5-methyl-3-((1-methyl-1H-benzo[d]imidazol-2-yl)methylene)indolin-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
79% With piperidine; In ethanol;Reflux; General procedure: To a mixture of oxindole (3a-f, 0.3mmol), 1-alkyl-1H benzo[d]imidazole-2-carbaldehydes (7a-e, 0.33mmol) in ethanol (2mL), was added catalytic amount of piperidine. The reaction mixture was stirred at reflux until complete consumption of the oxindole observed by TLC. After cooling, the precipitate was filtered, washed with cold ethanol, and dried in air to furnish pure (E)-benzo[d]imidazol-2-yl)methylene)indolin-2-ones 8a-z orange/yellow solids in moderate to good yields. Compounds 8c, 8f, 8i, 8l and 8o did not precipitated out from ethanol, were purified by column chromatography with silica gel (60-120) by using ethyl acetate:hexane (2:8 to 3:7). 4.1.1.13 (E)-5-Methyl-3-((1-methyl-1H-benzo[d]imidazol-2-yl)methylene)indolin-2-one (8m) Orange solid, Yield 79%; mp: 266-268 C; FT-IR: (cm-1): 3183, 3056, 2916, 1702, 1612, 1321, 815, 737; 1H NMR (500 MHz, DMSO-d6): δ 10.59 (brs, 1H, NH), 9.35 (s, 1H, Ar-H), 7.84 (d, J = 8.1 Hz, 1H, Ar-H), 7.69 (d, J = 8.1 Hz, 1H, Ar-H), 7.55 (s, 1H, C=CH), 7.41-7.31 (m, 2H, Ar-H), 7.15 (d, J = 7.8 Hz, 1H, Ar-H), 6.79 (d, J = 7.8 Hz, 1H, Ar-H), 4.02 (s, 3H, CH3), 2.35 (s, 3H, CH3); 13C NMR (75 MHz, CDCl3+DMSO-d6): δ 168.9, 147.5, 142.6, 141.0, 135.4, 131.4, 130.9, 129.9, 128.4, 123.9, 122.7, 120.9, 119.5, 117.3, 110.4, 109.1, 30.0, 20.8; HRMS (ESI): m/z calcd for C18H16N3O 290.1293, found 290.1279 [M+H]+; Purity: 99.2%.
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