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[ CAS No. 423165-33-7 ] {[proInfo.proName]}

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Chemical Structure| 423165-33-7
Chemical Structure| 423165-33-7
Structure of 423165-33-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 423165-33-7 ]

CAS No. :423165-33-7 MDL No. :MFCD03790890
Formula : C8H8BrNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :ZALXYXWTUXLPBJ-UHFFFAOYSA-N
M.W : 246.06 Pubchem ID :22832075
Synonyms :

Calculated chemistry of [ 423165-33-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.26
TPSA : 55.05 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 2.96
Log Po/w (WLOGP) : 2.76
Log Po/w (MLOGP) : 2.49
Log Po/w (SILICOS-IT) : 0.68
Consensus Log Po/w : 2.17

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.37
Solubility : 0.104 mg/ml ; 0.000423 mol/l
Class : Soluble
Log S (Ali) : -3.78
Solubility : 0.0409 mg/ml ; 0.000166 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.17
Solubility : 0.167 mg/ml ; 0.000679 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.19

Safety of [ 423165-33-7 ]

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 [ 423165-33-7 ]

* 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 [ 423165-33-7 ]

[ 423165-33-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52427-05-1 ]
  • [ 75-03-6 ]
  • [ 423165-33-7 ]
YieldReaction ConditionsOperation in experiment
91% With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; for 4h; To a mixture of <strong>[52427-05-1]2-bromo-5-nitrophenol</strong> (1.0 g, 4.59 mmol) and potassium carbonate (1.59 g, 11.5 mmol) in DMF (10 mL), was added iodomethane (1.79 g, 11.5 mmol). The reaction mixture was stirred at 70 °C for 4 h, then was cooled to rt. The mixture was diluted with water (100 mL) and extracted with EtOAc (2 x 75 mL).Combined organic extracts were washed with water and brine, dried over Na2SO4 andconcentrated to give Intermediate 8A (1.10 g, 4.18 mmol, 91percent yield). MS(ESI) m/z:248.0 (M+H) ?H NMR (300 MHz, DMSO-d6) oe ppm 7.90 (d, J = 8.6 Hz, 1 H), 7.81 (d,J = 2.5 Hz, 1 H), 7.78 - 7.73 (m, 1 H), 4.27 (q, J = 7.0 Hz, 2 H), 1.40 (t, J = 7.0 Hz, 3 H).
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