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[ CAS No. 171364-80-0 ] {[proInfo.proName]}

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Chemical Structure| 171364-80-0
Chemical Structure| 171364-80-0
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Product Details of [ 171364-80-0 ]

CAS No. :171364-80-0 MDL No. :MFCD02179438
Formula : C14H19BO4 Boiling Point : -
Linear Structure Formula :CH3O2CC6H4B(O2C2(CH3)4) InChI Key :REIZEQZILPXYKS-UHFFFAOYSA-N
M.W : 262.11 Pubchem ID :2773500
Synonyms :

Calculated chemistry of [ 171364-80-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 74.2
TPSA : 44.76 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.76
Log Po/w (WLOGP) : 1.77
Log Po/w (MLOGP) : 1.54
Log Po/w (SILICOS-IT) : 1.77
Consensus Log Po/w : 1.57

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.24
Solubility : 0.151 mg/ml ; 0.000576 mol/l
Class : Soluble
Log S (Ali) : -3.36
Solubility : 0.116 mg/ml ; 0.000441 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.08
Solubility : 0.022 mg/ml ; 0.0000839 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.86

Safety of [ 171364-80-0 ]

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 [ 171364-80-0 ]

* 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 [ 171364-80-0 ]

[ 171364-80-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 474706-74-6 ]
  • [ 171364-80-0 ]
  • [ 474706-76-8 ]
YieldReaction ConditionsOperation in experiment
With potassium phosphate;tetrakis(triphenylphosphine) palladium(0); In DMF (N,N-dimethyl-formamide); at 100℃; Production Example 51 methyl 4-(6-bromoimidazo[1,2-a]pyridin-3-yl)benzoate 2.3 g methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate prepared according to T. Ishiyama et al., J. Org. Chem., 60, 7508 (1995), 2.0 g <strong>[474706-74-6]6-bromo-3-iodoimidazo[1,2-a]pyridine</strong> (compound in Production Example 49), 2. 5 g potassiumphosphate, 360 mg tetrakistriphenyl phosphine palladium and 30 ML N, N-dimethylformamide were heated at 100C under nitrogen atmosphere.. Insolubles were filtered off, the solvent was removed, and the residue was purified by NH silica gel column chromatography (hexane/ethyl acetate) and recrystallized from ethyl acetate to give 1.39 g of the title compound (colorless crystals).1H-NMR (CDCl3) delta: 3.97(s, 3H), 7.32(dd, J=9.6, 2.0Hz, 1H), 7.62(d, J=9.6Hz, 1H), 7.65(dt, J=8.8, 2.0Hz, 2H), 7.79(br.s, 1H), 8.21(dt, J=8.8, 2.0Hz, 2H), 8.50(br.s, 1H)
  • 2
  • [ 1000623-95-9 ]
  • [ 171364-80-0 ]
  • methyl 4-(5-(4-(5-bromothiophen-2-yl)-2,5-bis(2-ethylhexyl)-3,6-dioxo-2,3,5,6-tetrahydropyrro lo[3,4-c]pyrrol-1-yl)thiophen-2-yl)benzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
72.7% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In water; toluene; at 100℃; for 24h;Inert atmosphere; A mixture of 3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-ethylhexyl)-2,5-dihydropyrrolo[3,4-c] pyrrole-1,4-dione (5) (1.97 g,2.90 mmol), methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (6) (0.76 g, 2.90 mmol), K2CO3 (1.60 g, 11.60 mmol),Pd(PPh3)4 (0.17 g, 5 mol%) and toluene/H2O (60 mL, 3/1, V/V) wasadded to the reaction flask under a N2 atmosphere and then stirred at100 C for 24 h. After cooling to the room temperature, the reactionmixture was extracted with CH2Cl2, washed with water and brine,and dried over MgSO4. The crude product was purified by columnchromatography (CH2Cl2/petroleum ether, 1/4, V/V) on silica gel toyield a purplish red solid (1.55 g, yield 72.7%). 1H NMR (400 MHz,CDCl3, delta/ppm): 8.97 (d, J = 4.2,1H), 8.11 (d, J = 8.5, 3H), 7.76 (d, J = 4.5,3H), 7.58 (d, J = 4.3, 1H), 4.11-4.04 (m, 3H), 3.96 (s, 4H), 1.93 (s, 2H),1.42-1.26 (m, 16H), 0.94-0.83 (m, 12H). MALDI-TOF MS (m/z): calcdfor (C76H75N3O4S3): 736.2004; Found: 736.2350.
  • 3
  • [ 68857-86-3 ]
  • [ 171364-80-0 ]
  • methyl 5'-ethyl-2'-isobutyrylbiphenyl-4-carboxylate [ No CAS ]
  • 4
  • [ 1202-25-1 ]
  • [ 73183-34-3 ]
  • [ 333-27-7 ]
  • [ 171364-80-0 ]
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; ;