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[ CAS No. 19833-96-6 ] {[proInfo.proName]}

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Chemical Structure| 19833-96-6
Chemical Structure| 19833-96-6
Structure of 19833-96-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 19833-96-6 ]

CAS No. :19833-96-6 MDL No. :MFCD00019295
Formula : C14H18O3 Boiling Point : -
Linear Structure Formula :- InChI Key :FGMUSNHTKNGVQD-UHFFFAOYSA-N
M.W : 234.29 Pubchem ID :89233
Synonyms :

Calculated chemistry of [ 19833-96-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 65.27
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.61
Log Po/w (XLOGP3) : 2.81
Log Po/w (WLOGP) : 2.13
Log Po/w (MLOGP) : 2.12
Log Po/w (SILICOS-IT) : 2.55
Consensus Log Po/w : 2.44

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.06
Solubility : 0.204 mg/ml ; 0.000871 mol/l
Class : Soluble
Log S (Ali) : -3.44
Solubility : 0.0842 mg/ml ; 0.00036 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.11
Solubility : 0.181 mg/ml ; 0.000773 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.55

Safety of [ 19833-96-6 ]

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 [ 19833-96-6 ]

* 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 [ 19833-96-6 ]

[ 19833-96-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13220-33-2 ]
  • [ 19833-96-6 ]
  • [ 13118-11-1 ]
YieldReaction ConditionsOperation in experiment
72% With sodium; In n-heptane; for 3h; A solution of 2 (2.20 g, 9.4 mmol) and N-methyl-3-pyrrolidinol (3, 1.30 g, 13 mmol) in 40 ml of n-heptane was heated until 20 ml of heptane had been distilled. About 0.003 g of sodium was added, and the solution was stirred and heated for 2 h as the distillation was continued. More heptane was added at such a rate as to keep the reaction volume constant. Additional sodium was added at the end of an hour. The solution was then cooled and extracted with 3N HCl. The acid extract was made alkaline with concentrated NaOH and extracted three times with ether. Removal of the dried ether solution gave a crude oil. Flash chromatography of the crude product on silica gel with 8:1 EtOAc:EtOH gave pure product 4 (2.053 g, 72percent). Analysis for C18H25NO3. Calcd: C, 71.26; H, 8.31; N, 4.62. Found: C, 71.55; H, 8.44; N, 4.68. 1H NMR(CDCl3, 500 MHz): 1.27-1.35, 1.40-1.47, 1.54-1.60, 1.75-1.90 [8H, m, (CH2)4], 2.12-2.30, 2.52-2.57, 2.64-2.81 (6H, m CH2NCH2CH2), 2.33, 2.36 (3H, 2s, NCH3), 2.93 [(1H, p, CHC(OH)], 3.83 (1H, bs, OH), 5.23 (1H, m, CO2CH), 7.23-7.36, 7.64-7.67 (5H, m, Ph) ppm.
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