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[ CAS No. 153898-63-6 ] {[proInfo.proName]}

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Chemical Structure| 153898-63-6
Chemical Structure| 153898-63-6
Structure of 153898-63-6 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Frey, Brandon L. ; Thai, Phong ; Patel, Lauv , et al. DOI:

Abstract: The design and optimization of novel electrocatalysts requires robust structure-activity data to correlate catalyst structure with electrochem. behavior. Aryl iodides have been gaining attention as metal-free electrocatalysts but exptl. data are available for only a limited set of structures. Herein we report electrochem. data for a family of 70 aryl iodides. Half-peak potentials are utilized as proxies for reduction potentials and reveal that, despite differences in electrochem. reversibility, the potential for one-electron oxidation of 4-substituted aryl iodides to the corresponding iodanyl radicals is well-correlated with standard Hammett parameters. Addnl. data are presented for 3- and 2-substituted aryl iodides, including structures with potentially chelating 2-substituents that are commonly encountered in hypervalent iodine reagents. Finally, potential decomposition processes relevant to the (in)stability of iodanyl radicals are presented. We anticipate that the collected data will advance the design and application of aryl iodide electrocatalysis.

Keywords: hypervalent iodine ; electrochemistry ; linear free-energy relationships ; sustainable catalysis ; oxidation

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Product Details of [ 153898-63-6 ]

CAS No. :153898-63-6 MDL No. :MFCD08458361
Formula : C7H8INO Boiling Point : -
Linear Structure Formula :- InChI Key :CYDBBGSUZRDOPE-UHFFFAOYSA-N
M.W : 249.05 Pubchem ID :11139508
Synonyms :

Calculated chemistry of [ 153898-63-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.06
TPSA : 35.25 ?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) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 1.86
Log Po/w (WLOGP) : 1.89
Log Po/w (MLOGP) : 2.06
Log Po/w (SILICOS-IT) : 2.07
Consensus Log Po/w : 1.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.93
Solubility : 0.29 mg/ml ; 0.00116 mol/l
Class : Soluble
Log S (Ali) : -2.22
Solubility : 1.5 mg/ml ; 0.006 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.12
Solubility : 0.188 mg/ml ; 0.000757 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 153898-63-6 ]

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 [ 153898-63-6 ]

* 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 [ 153898-63-6 ]

[ 153898-63-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 153898-63-6 ]
  • [ 191171-55-8 ]
  • [ 6933-49-9 ]
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