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[ CAS No. 929301-99-5 ] {[proInfo.proName]}

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Chemical Structure| 929301-99-5
Chemical Structure| 929301-99-5
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Product Details of [ 929301-99-5 ]

CAS No. :929301-99-5 MDL No. :MFCD11111843
Formula : C19H28N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :MTPQMAJDIOUCHT-UHFFFAOYSA-N
M.W : 316.44 Pubchem ID :45790087
Synonyms :

Calculated chemistry of [ 929301-99-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 23
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.63
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 99.94
TPSA : 32.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.79
Log Po/w (XLOGP3) : 3.02
Log Po/w (WLOGP) : 2.61
Log Po/w (MLOGP) : 2.9
Log Po/w (SILICOS-IT) : 2.79
Consensus Log Po/w : 3.02

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.57
Solubility : 0.0857 mg/ml ; 0.000271 mol/l
Class : Soluble
Log S (Ali) : -3.37
Solubility : 0.134 mg/ml ; 0.000423 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.28
Solubility : 0.0165 mg/ml ; 0.0000521 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.84

Safety of [ 929301-99-5 ]

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

Application In Synthesis of [ 929301-99-5 ]

* 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 [ 929301-99-5 ]

[ 929301-99-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 929301-99-5 ]
  • [ 929302-18-1 ]
YieldReaction ConditionsOperation in experiment
Preparation of compound 4A mixture of compound 3 (1.3 g, 4.11 mmol) and Pd(OH)2 (200 mg) in 15 mL of MeOH was stirred under 55 psi of H2 at 35 0C overnight. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in DCM, dried over anhydrous Na2SO4 and concentrated. The residue was dissolved in anhydrous ether, then HCl(g)/MeOH was added dropwise until pH = 6-7. The mixture was filtered to afford compound 4 (0.95 g). 1H NMR (CD4O, HCl salt) delta: 3.72 (s, 4 H), 3.30 (t, 4 H), 1.99 (t 4 H), 1.43 (9 H).
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