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[ CAS No. 29897-82-3 ] {[proInfo.proName]}

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Chemical Structure| 29897-82-3
Chemical Structure| 29897-82-3
Structure of 29897-82-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 29897-82-3 ]

CAS No. :29897-82-3 MDL No. :MFCD00127807
Formula : C11H15N Boiling Point : No data available
Linear Structure Formula :- InChI Key :CWEGCQIIDCZZED-UHFFFAOYSA-N
M.W : 161.24 Pubchem ID :122501
Synonyms :

Calculated chemistry of [ 29897-82-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.45
Num. rotatable bonds : 2
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 55.33
TPSA : 3.24 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 2.28
Log Po/w (WLOGP) : 1.75
Log Po/w (MLOGP) : 2.39
Log Po/w (SILICOS-IT) : 2.71
Consensus Log Po/w : 2.33

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.51
Solubility : 0.494 mg/ml ; 0.00306 mol/l
Class : Soluble
Log S (Ali) : -1.99
Solubility : 1.67 mg/ml ; 0.0103 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.24
Solubility : 0.0936 mg/ml ; 0.000581 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 29897-82-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 29897-82-3 ]

* 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 [ 29897-82-3 ]

[ 29897-82-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2142-06-5 ]
  • [ 29897-82-3 ]
YieldReaction ConditionsOperation in experiment
82% With 1,1,3,3-Tetramethyldisiloxane; tris(pentafluorophenyl)borate; In 1,4-dioxane; at 110℃; for 16h;Inert atmosphere; Schlenk technique; General procedure: To the mixture of B(C6F5)3 (5.0mol%) and cyclic imides (1.0mmol) in dioxane, was added PhSiH3 (3.0mmol) slowly under an atmosphere of nitrogen. The reaction mixture was stirred and refluxed at 110C under an atmosphere of nitrogen. After the imide was consumed completely (detected by TLC) the mixture was added with aqueous ammonia (15mL) and extracted with CH2Cl2 (10mL×3). The combined organic phase was dried over Na2SO4, after removing the solvent under vacuum, the residue was purified by column chromatography to give the product.
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