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[ CAS No. 106120-04-1 ] {[proInfo.proName]}

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Chemical Structure| 106120-04-1
Chemical Structure| 106120-04-1
Structure of 106120-04-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 106120-04-1 ]

CAS No. :106120-04-1 MDL No. :MFCD16293393
Formula : C6H5BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HYHHGFFTWSYNMV-UHFFFAOYSA-N
M.W : 189.01 Pubchem ID :557383
Synonyms :

Calculated chemistry of [ 106120-04-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.19
TPSA : 40.46 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.27
Log Po/w (XLOGP3) : 1.21
Log Po/w (WLOGP) : 1.86
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 1.58
Consensus Log Po/w : 1.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.27
Solubility : 1.02 mg/ml ; 0.0054 mol/l
Class : Soluble
Log S (Ali) : -1.66
Solubility : 4.17 mg/ml ; 0.0221 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.1
Solubility : 1.5 mg/ml ; 0.00793 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.47

Safety of [ 106120-04-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 106120-04-1 ]

* 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 [ 106120-04-1 ]

[ 106120-04-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 16618-68-1 ]
  • [ 106120-04-1 ]
  • 2
  • [ 3970-39-6 ]
  • [ 106120-04-1 ]
  • C13H10BrNO5 [ No CAS ]
  • 3
  • [ 3970-39-6 ]
  • [ 106120-04-1 ]
  • 2-(3-bromo-5-hydroxyphenoxy)-3-nitrophenol [ No CAS ]
  • 4
  • [ 19346-46-4 ]
  • [ 106120-04-1 ]
  • 2,2'-(5-bromo-1,3-phenylene)bis(oxy)bis(3-methyl-5-nitropyridine) [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; at 20℃; for 16h; Potassium Carbonate was added to a solution of 5-bromobenzene-1,3-diol and <strong>[19346-46-4]2-fluoro-3-methyl-5-nitropyridine</strong> and stirred at room temperature for 16 hours. Reaction mixture was diluted with ice cold water and extracted with ethyl acetate. The combined organic layer was dried with sodium sulphate and evaporated under reduced pressure to obtain 2,2'-(5-bromo-1,3-phenylene)bis(oxy)bis(3-methyl-5-nitropyridine).
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