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[ CAS No. 1758-46-9 ] {[proInfo.proName]}

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Chemical Structure| 1758-46-9
Chemical Structure| 1758-46-9
Structure of 1758-46-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1758-46-9 ]

CAS No. :1758-46-9 MDL No. :MFCD00052975
Formula : C8H11NO Boiling Point : -
Linear Structure Formula :- InChI Key :IMLAIXAZMVDRGA-UHFFFAOYSA-N
M.W : 137.18 Pubchem ID :15651
Synonyms :

Calculated chemistry of [ 1758-46-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.82
TPSA : 21.26 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : -3.77
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : 1.12
Log Po/w (MLOGP) : 1.21
Log Po/w (SILICOS-IT) : 1.3
Consensus Log Po/w : 0.15

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.5
Solubility : 4.33 mg/ml ; 0.0318 mol/l
Class : Very soluble
Log S (Ali) : -0.93
Solubility : 15.9 mg/ml ; 0.117 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.56
Solubility : 0.377 mg/ml ; 0.00277 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 1758-46-9 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2735
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1758-46-9 ]

* 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 [ 1758-46-9 ]

[ 1758-46-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1758-46-9 ]
  • [ 51997-51-4 ]
  • 1-[carbazolyl-(4)-oxy]-3-(2-phenoxyethylamino)-propan-2-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% (a) 1-[carbazolyl-(4)-oxy]-3-(2-phenoxyethylamino)-propan-2-ol yield 32% of theory; m.p. 105-107 C., from 4-(2,3-epoxypropoxy)-carbazole and 2-phenoxyethylamine.
  • 2
  • [ 1758-46-9 ]
  • [ 51997-51-4 ]
  • [ 72956-10-6 ]
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