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[ CAS No. 4837-90-5 ] {[proInfo.proName]}

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Chemical Structure| 4837-90-5
Chemical Structure| 4837-90-5
Structure of 4837-90-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4837-90-5 ]

CAS No. :4837-90-5 MDL No. :MFCD00009737
Formula : C9H9NO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 147.17 Pubchem ID :-
Synonyms :
Chemical Name :4-Methoxy-1H-indole

Calculated chemistry of [ 4837-90-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.79
TPSA : 25.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 2.0
Log Po/w (WLOGP) : 2.18
Log Po/w (MLOGP) : 1.23
Log Po/w (SILICOS-IT) : 2.53
Consensus Log Po/w : 1.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.55
Solubility : 0.413 mg/ml ; 0.00281 mol/l
Class : Soluble
Log S (Ali) : -2.15
Solubility : 1.04 mg/ml ; 0.00705 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.39
Solubility : 0.06 mg/ml ; 0.000407 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.3

Safety of [ 4837-90-5 ]

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 [ 4837-90-5 ]

* 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 [ 4837-90-5 ]

[ 4837-90-5 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 22630-08-6 ]
  • [ 4837-88-1 ]
  • [ 4837-90-5 ]
  • 2
  • [ 4837-88-1 ]
  • [ 4637-24-5 ]
  • [ 4837-90-5 ]
  • 3
  • [ 4837-90-5 ]
  • [ 26638-43-7 ]
  • 2-(4-methoxy-indole-1-sulfonyl)-benzoic acid methyl ester [ No CAS ]
  • 5
  • [ 4837-90-5 ]
  • [ 406938-53-2 ]
  • 6
  • [ 112970-44-2 ]
  • [ 4837-90-5 ]
  • 7
  • [ 4837-90-5 ]
  • [ 14135-38-7 ]
  • [ 530116-20-2 ]
YieldReaction ConditionsOperation in experiment
85% Compound 1 (3 g, 0.026 mol) was dissolved in DMF (150 mL), and cooled to 0° C. NaH (dry, 95percent, 0.97 g, 0.038 mol) was added, and the reaction was stirred for 15 min. A solution of 2-fluorophenyl disulphide (6.5 g, 0.026 mol) in DMF (5 mL) was added, and the reaction was allowed to proceed at r.t. overnight. The reaction was quenched with H2O. Solvent was removed. CH2Cl2 was added to dilution the reaction mixture. The organics were extracted with brine (50 ml.x.2) and H2O (50 ml.x.2). The organic layer was dried over Na2SO4 and concentrated to dryness. The crude product was purified via (10percent EtOAc/hexanes) to give 5.33 g (85percent) of compound 2 as a white solid.
  • 9
  • [ 4837-90-5 ]
  • [ 3471-31-6 ]
  • 5-methoxy-3-((4-methoxy-1H-indol-3-yl)methyl)-1H-indole [ No CAS ]
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