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[ CAS No. 16851-82-4 ] {[proInfo.proName]}

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Chemical Structure| 16851-82-4
Chemical Structure| 16851-82-4
Structure of 16851-82-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 16851-82-4 ]

CAS No. :16851-82-4 MDL No. :MFCD00067739
Formula : C10H9NO2S Boiling Point : -
Linear Structure Formula :- InChI Key :PPPXRIUHKCOOMU-UHFFFAOYSA-N
M.W : 207.25 Pubchem ID :140146
Synonyms :

Calculated chemistry of [ 16851-82-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 53.5
TPSA : 47.45 ?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) : -6.22 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 1.89
Log Po/w (WLOGP) : 2.81
Log Po/w (MLOGP) : 2.07
Log Po/w (SILICOS-IT) : 0.81
Consensus Log Po/w : 1.9

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.77
Solubility : 0.356 mg/ml ; 0.00172 mol/l
Class : Soluble
Log S (Ali) : -2.51
Solubility : 0.642 mg/ml ; 0.0031 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.23
Solubility : 0.122 mg/ml ; 0.000589 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.12

Safety of [ 16851-82-4 ]

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 [ 16851-82-4 ]

* 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 [ 16851-82-4 ]

[ 16851-82-4 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 16851-82-4 ]
  • [ 5919-26-6 ]
  • [ 5930-94-9 ]
  • [ 97188-21-1 ]
  • 3
  • [ 16851-82-4 ]
  • [ 104-21-2 ]
  • [ 1301740-46-4 ]
YieldReaction ConditionsOperation in experiment
98%Chromat. With trifluorormethanesulfonic acid; at 20℃; for 0.0833333h;Neat (no solvent); General procedure: 430 muL of anisyl acetate (2.5 mmol, 1 equiv) and 2.2 mL of anisole (12.25 mmol, 5 equiv) were placed into a 10 mL round-bottom flask equipped with a magnetic stir-bar. Then 11 muL 5% of pure triflic acid (0.125 mmol) was added and the solution was stirred for 20 min. The crude was analyzed by 1H NMR and GC-MS. Purification by column chromatography gave 484 mg (85% yield) of bis(4-methoxyphenyl)methane, which was identical to an authentic sample.
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