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[ CAS No. 41532-84-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 41532-84-7
Chemical Structure| 41532-84-7
Structure of 41532-84-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 41532-84-7 ]

CAS No. :41532-84-7 MDL No. :MFCD00082627
Formula : C15H15N Boiling Point : -
Linear Structure Formula :- InChI Key :WJZSZXCWMATYFX-UHFFFAOYSA-N
M.W : 209.29 Pubchem ID :170530
Synonyms :
Chemical Name :1,1,2-Trimethyl-1H-benzo[e]indole

Calculated chemistry of [ 41532-84-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.27
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 73.64
TPSA : 12.36 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.07 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.6
Log Po/w (XLOGP3) : 3.53
Log Po/w (WLOGP) : 3.84
Log Po/w (MLOGP) : 3.43
Log Po/w (SILICOS-IT) : 4.88
Consensus Log Po/w : 3.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.82
Solubility : 0.0314 mg/ml ; 0.00015 mol/l
Class : Soluble
Log S (Ali) : -3.47
Solubility : 0.0703 mg/ml ; 0.000336 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.81
Solubility : 0.000321 mg/ml ; 0.00000153 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.88

Safety of [ 41532-84-7 ]

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 [ 41532-84-7 ]

* 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 [ 41532-84-7 ]

[ 41532-84-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 41532-84-7 ]
  • [ 49827-15-8 ]
  • [ 1227799-21-4 ]
  • 2
  • [ 563-80-4 ]
  • [ 2243-58-5 ]
  • [ 41532-84-7 ]
YieldReaction ConditionsOperation in experiment
With acetic acid; at 100℃; for 24h; General procedure: In parallel, substituted hydrazines 1 (4.0 g, 22.25 mmol) were reacted with 3-methylbutanone(3 mL, 28.04 mmol) in acetic acid and heated to a 100 C for 24 h. The solution was then neutralizedusing sodium bicarbonate and extracted using dichloromethane; affording substituted indolenineheterocycles 2 which was dried under reduced pressure. The heterocycles 2 were then reacted withan alkyl halide in acetonitrile at 100 C for 12-18 h. The quaternary ammonium salts 3 were precipitatedwith diethyl ether, and collected.
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