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[ CAS No. 4771-49-7 ] {[proInfo.proName]}

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Chemical Structure| 4771-49-7
Chemical Structure| 4771-49-7
Structure of 4771-49-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4771-49-7 ]

CAS No. :4771-49-7 MDL No. :MFCD00049347
Formula : C10H9NO Boiling Point : -
Linear Structure Formula :- InChI Key :LZERQSJGPXFAKB-UHFFFAOYSA-N
M.W : 159.18 Pubchem ID :4777902
Synonyms :

Calculated chemistry of [ 4771-49-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.65
TPSA : 32.86 ?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) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.46
Log Po/w (XLOGP3) : 1.88
Log Po/w (WLOGP) : 2.29
Log Po/w (MLOGP) : 1.18
Log Po/w (SILICOS-IT) : 3.13
Consensus Log Po/w : 1.99

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.5
Solubility : 0.503 mg/ml ; 0.00316 mol/l
Class : Soluble
Log S (Ali) : -2.19
Solubility : 1.02 mg/ml ; 0.00642 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.61
Solubility : 0.0393 mg/ml ; 0.000247 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.18

Safety of [ 4771-49-7 ]

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 [ 4771-49-7 ]

* 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 [ 4771-49-7 ]

[ 4771-49-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 79-24-3 ]
  • [ 4771-49-7 ]
  • [ 566200-36-0 ]
  • 2
  • [ 4771-49-7 ]
  • [ 940304-80-3 ]
YieldReaction ConditionsOperation in experiment
With hydroxylamine hydrochloride; sodium acetate; In ethanol; at 22℃; for 3h; 10.1. To a solution of <strong>[4771-49-7]6-methyl-1H-indole-3-carbaldehyde</strong> (0.96 g, Lit. 5) in ethanol (30 ml) was added at 22° C. hydroxylamine hydrochloride (0.46 g) and sodium acetate (0.54 g) and the mixture was stirred for 3 h. The mixture was evaporated and the residue triturated with water and dichloromethane/n-heptane (1:1) and dried to give <strong>[4771-49-7]6-methyl-1H-indole-3-carbaldehyde</strong> oxime (0.96 g) as a pink solid. MS: 175.3 ([M+H]+).
  • 3
  • [ 4771-49-7 ]
  • 2,4,6-trimethyl-N-[1-methyl-2-(6-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide [ No CAS ]
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