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[ CAS No. 578729-21-2 ] {[proInfo.proName]}

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Chemical Structure| 578729-21-2
Chemical Structure| 578729-21-2
Structure of 578729-21-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 578729-21-2 ]

CAS No. :578729-21-2 MDL No. :MFCD11506010
Formula : C13H18BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :KECPRZHCNCDSET-SECBINFHSA-N
M.W : 300.19 Pubchem ID :52987808
Synonyms :

Calculated chemistry of [ 578729-21-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.46
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 72.46
TPSA : 38.33 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.39
Log Po/w (XLOGP3) : 3.52
Log Po/w (WLOGP) : 3.71
Log Po/w (MLOGP) : 3.32
Log Po/w (SILICOS-IT) : 2.95
Consensus Log Po/w : 3.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.85
Solubility : 0.0424 mg/ml ; 0.000141 mol/l
Class : Soluble
Log S (Ali) : -4.01
Solubility : 0.0294 mg/ml ; 0.000098 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.62
Solubility : 0.00712 mg/ml ; 0.0000237 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.41

Safety of [ 578729-21-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 578729-21-2 ]

* 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.

  • Upstream synthesis route of [ 578729-21-2 ]

[ 578729-21-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 578729-21-2 ]
  • [ 73183-34-3 ]
  • [ 578729-05-2 ]
YieldReaction ConditionsOperation in experiment
7.8 g With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In 1,4-dioxane at 90℃; (R)-4-(1-((tert-Butoxycarbonyl)amino)ethyl)bromobenzene (4 g, 13.3 mmol) was placed in 25 mL of dioxane solution.Add KOAc (2.7 g, 26.7 mmol), bis(pinacolato)diboron (4 g, 15.34 mmol),PdCl 2 (dppf) (500 mg, 0.67 mmol) was reacted at 90 ° C overnight.The reaction solution was concentrated, dissolved in petroleum ether containing 20percent ethyl acetate, and the solution was brown, and the glass-glass funnel was filled with about 20 g of 300 mesh silica gel.The reaction solution was filtered through a silica gel column to remove dark impurities, and the filter cake was washed with the same ratio of solvent.To give a pale yellow solution, the solvent was removed under reduced pressure, to give 7.8 g orange oil,Yield >100percent.
Reference: [1] Patent: WO2005/63690, 2005, A1, . Location in patent: Page/Page column 28
[2] Patent: US2003/220375, 2003, A1,
[3] European Journal of Medicinal Chemistry, 2019, p. 407 - 422
[4] Patent: CN109761902, 2019, A, . Location in patent: Paragraph 0094; 0099-0101
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