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[ CAS No. 13472-60-1 ] {[proInfo.proName]}

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Chemical Structure| 13472-60-1
Chemical Structure| 13472-60-1
Structure of 13472-60-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 13472-60-1 ]

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Product Details of [ 13472-60-1 ]

CAS No. :13472-60-1 MDL No. :MFCD05663709
Formula : C6H5Br2NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :MBMQYTQCUCQJEH-UHFFFAOYSA-N
M.W : 266.92 Pubchem ID :13567752
Synonyms :

Calculated chemistry of [ 13472-60-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.13
TPSA : 22.12 ?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) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.46
Log Po/w (XLOGP3) : 2.54
Log Po/w (WLOGP) : 2.62
Log Po/w (MLOGP) : 2.08
Log Po/w (SILICOS-IT) : 2.71
Consensus Log Po/w : 2.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.47
Solubility : 0.0898 mg/ml ; 0.000336 mol/l
Class : Soluble
Log S (Ali) : -2.65
Solubility : 0.596 mg/ml ; 0.00223 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.86
Solubility : 0.037 mg/ml ; 0.000139 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.88

Safety of [ 13472-60-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13472-60-1 ]

* 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 [ 13472-60-1 ]

[ 13472-60-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 13472-60-1 ]
  • [ 40360-47-2 ]
  • 2
  • [ 13472-60-1 ]
  • [ 68-12-2 ]
  • [ 65873-73-6 ]
  • [ 103058-87-3 ]
  • 3
  • [ 75806-85-8 ]
  • [ 13472-60-1 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; Referential Example 11. 3,5-Dibromo-2-methoxypyridine 80ml of a 28% sodium methoxide solution was incorporated with 30.0g of <strong>[75806-85-8]2,3,5-tribromopyridine</strong> under ice-cooling, followed by stirring at 50C for 2 hours. The reaction solution was diluted with water and extracted with diethyl ether. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (ethyl acetate/hexane=1:20), to give 18.5g of the title compound. 1H-NMR (400MHz, CDCl3); δ(ppm) 3.99(s,3H), 7.93(d,1H), 8.14(d,1H).
  • 4
  • [ 67-56-1 ]
  • [ 75806-85-8 ]
  • [ 13472-60-1 ]
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