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[ CAS No. 10035-16-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 10035-16-2
Chemical Structure| 10035-16-2
Structure of 10035-16-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 10035-16-2 ]

CAS No. :10035-16-2 MDL No. :MFCD03411182
Formula : C9H6O2 Boiling Point : -
Linear Structure Formula :- InChI Key :LLLBDLDNTMMZHL-UHFFFAOYSA-N
M.W : 146.14 Pubchem ID :2773875
Synonyms :

Calculated chemistry of [ 10035-16-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.6
TPSA : 30.21 ?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) : -5.92 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 1.79
Log Po/w (WLOGP) : 2.25
Log Po/w (MLOGP) : 0.88
Log Po/w (SILICOS-IT) : 2.56
Consensus Log Po/w : 1.82

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.41
Solubility : 0.564 mg/ml ; 0.00386 mol/l
Class : Soluble
Log S (Ali) : -2.04
Solubility : 1.32 mg/ml ; 0.00906 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.21
Solubility : 0.0895 mg/ml ; 0.000612 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.85

Safety of [ 10035-16-2 ]

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 [ 10035-16-2 ]

* 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.

  • Downstream synthetic route of [ 10035-16-2 ]

[ 10035-16-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 423768-52-9 ]
  • [ 10035-16-2 ]
  • [ 1185322-46-6 ]
YieldReaction ConditionsOperation in experiment
63% To a solution of benzofuran-5-carbaldehyde (526 mg, 3.6 mmol, 1.2 equiv) in MeOH (15 mL) were added NaOAc (246 mg, 3.0 mmol, 1.0 equiv), HOAc (172 muL, 3.0 mmol, 1.0 equiv) and (l,5-dimethyl-l-pyrazole-3-yl)methylamine (376 mg, 3.0 mmol, 1.0 equiv., available from Maybridge). The mixture was stirred at room temperature for 5 min, and then treated with NaBH4 (273 mg, 7.2 mmol, 2.4 equiv) at 0 0C. The resulting mixture <n="52"/>was allowed to return to room temperature and stirred for 1 h, after which time the reaction was quenched with IN NaOH. The mixture was concentrated in vacuo to remove most of the MeOH, and the water layer was extracted with ethyl acetate three times. The combined organic phase was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified on silica gel with ethyl acetate/dichloromethane/methanol 5/5/1 as eluant to afford l-(Benzofuran-5-yl)-N-((l,5-dimethyl-lH-pyrazol-3-yl)methyl)methanamine (478 mg, 63%). MS 256 (MH)+. Purity 95% (HPLC)
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