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[ CAS No. 22884-95-3 ] {[proInfo.proName]}

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Chemical Structure| 22884-95-3
Chemical Structure| 22884-95-3
Structure of 22884-95-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 22884-95-3 ]

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Product Details of [ 22884-95-3 ]

CAS No. :22884-95-3 MDL No. :MFCD00016380
Formula : C9H9N Boiling Point : -
Linear Structure Formula :NCC6H3(CH3)2 InChI Key :OWISXYQFTOYGRO-UHFFFAOYSA-N
M.W : 131.17 Pubchem ID :89884
Synonyms :

Calculated chemistry of [ 22884-95-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.09
TPSA : 23.79 ?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) : -5.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.03
Log Po/w (XLOGP3) : 2.24
Log Po/w (WLOGP) : 2.18
Log Po/w (MLOGP) : 2.1
Log Po/w (SILICOS-IT) : 2.74
Consensus Log Po/w : 2.26

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.51
Solubility : 0.407 mg/ml ; 0.0031 mol/l
Class : Soluble
Log S (Ali) : -2.38
Solubility : 0.553 mg/ml ; 0.00421 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.22
Solubility : 0.0789 mg/ml ; 0.000601 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.33

Safety of [ 22884-95-3 ]

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 [ 22884-95-3 ]

* 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 [ 22884-95-3 ]

[ 22884-95-3 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 95-47-6 ]
  • [ 143814-17-9 ]
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  • 2
  • [ 95-47-6 ]
  • mercury (II)-fulminate [ No CAS ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
  • 3
  • [ 22884-95-3 ]
  • [ 6575-13-9 ]
  • [ 5724-56-1 ]
  • 4
  • [ 583-71-1 ]
  • [ 68-12-2 ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
YieldReaction ConditionsOperation in experiment
20%; 74% General procedure: n-Butyllithium (1.67 M solution in hexane, 3.3 mL, 5.5 mmol) was added dropwise to a solution of p-bromotoluene (855 mg, 5.0 mmol) in THF (5 mL) at -70 C. After 30 min, the resulting mixture was warmed and stirred for 5 min at 0 C. Then, DMF (0.43 mL, 5.5 mmol) was added and the obtained mixture was stirred at 0 C. After 1 h at the same temperature, aq NH3 (10 mL, 150 mmol) and I2 (1.40 g, 5.5 mmol) were added and the obtained mixture was stirred for 2 h at rt. The reaction mixture was quenched with satd aq Na2SO3 (15 mL) and extracted with Et2O (3×20 mL). The organic layer was washed with brine and dried over Na2SO4 to provide 4-methylbenzonitrile in over 80% purity. The product was purified by a short column chromatography on silica gel (Hexane/EtOAc=9:1) to give pure 4-methylbenzonitrile in 80% yield as a colorless solid.
  • 5
  • [ 95-47-6 ]
  • (3,5-bis(trifluoromethyl)phenyl)(cyano)-l3-iodanyl trifluoromethanesulfonate [ No CAS ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
  • 6
  • [ 95-47-6 ]
  • [ 75-05-8 ]
  • [ 5724-56-1 ]
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  • 7
  • [ 330660-35-0 ]
  • [ 95-47-6 ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
  • 8
  • [ 95-47-6 ]
  • potassium hexacyanoferrate(III) [ No CAS ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
  • 9
  • potassiumhexacyanoferrate(II) trihydrate [ No CAS ]
  • [ 95-47-6 ]
  • [ 5724-56-1 ]
  • [ 22884-95-3 ]
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