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[ CAS No. 613-69-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 613-69-4
Chemical Structure| 613-69-4
Structure of 613-69-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 613-69-4 ]

CAS No. :613-69-4 MDL No. :MFCD00003316
Formula : C9H10O2 Boiling Point : -
Linear Structure Formula :- InChI Key :DUVJMSPTZMCSTQ-UHFFFAOYSA-N
M.W : 150.17 Pubchem ID :11950
Synonyms :

Calculated chemistry of [ 613-69-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.13
TPSA : 26.3 ?2

Pharmacokinetics

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

Lipophilicity

Log Po/w (iLOGP) : 2.03
Log Po/w (XLOGP3) : 2.09
Log Po/w (WLOGP) : 1.9
Log Po/w (MLOGP) : 1.44
Log Po/w (SILICOS-IT) : 2.31
Consensus Log Po/w : 1.95

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.29
Solubility : 0.764 mg/ml ; 0.00509 mol/l
Class : Soluble
Log S (Ali) : -2.27
Solubility : 0.802 mg/ml ; 0.00534 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.86
Solubility : 0.208 mg/ml ; 0.00138 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.17

Safety of [ 613-69-4 ]

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

Application In Synthesis of [ 613-69-4 ]

* 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 [ 613-69-4 ]

[ 613-69-4 ] Synthesis Path-Downstream   1~5

  • 3
  • [ 613-69-4 ]
  • [ 76-05-1 ]
  • [ 162167-97-7 ]
  • <i>C</i>-[1-(2-ethoxy-benzyl)-piperidin-3-yl]-methylamine; compound with trifluoro-acetic acid [ No CAS ]
  • 4
  • [ 613-69-4 ]
  • [ 4265-25-2 ]
  • 5
  • [ 613-69-4 ]
  • [ 65854-91-3 ]
  • [ 1292850-47-5 ]
YieldReaction ConditionsOperation in experiment
100% General procedure: N-Pivaloyl-4-chloroaniline (33, 595 mg, 2.81 mmol) was dissolved in THF (50 ml), and the solution was added sec-butyl lithium c-hexane, n-hexane solution (0.99 M, 5.96 ml, 6.18 mmol) at -78 C, and then stirred at 0 C for 2 h. The mixture was added 2-chloro-3-fluoro-benzaldehyde (490 mg, 3.09 mmol) at the same temperature for 30 min. The reaction mixture was poured saturated with NH4Claq and AcOEt. The organic layer was washed with brine and dried over Na2SO4. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (n-hexane/AcOEt = 9:1) to give the title compound (676 mg, 65%) as light yellow oil.
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