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[ CAS No. 2142-71-4 ] {[proInfo.proName]}

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Chemical Structure| 2142-71-4
Chemical Structure| 2142-71-4
Structure of 2142-71-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2142-71-4 ]

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Product Details of [ 2142-71-4 ]

CAS No. :2142-71-4 MDL No. :MFCD03844735
Formula : C10H12O Boiling Point : -
Linear Structure Formula :- InChI Key :YXJIYJZHAPHBHG-UHFFFAOYSA-N
M.W : 148.20 Pubchem ID :16505
Synonyms :

Calculated chemistry of [ 2142-71-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.57
TPSA : 17.07 ?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) : -5.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.05
Log Po/w (XLOGP3) : 2.33
Log Po/w (WLOGP) : 2.51
Log Po/w (MLOGP) : 2.4
Log Po/w (SILICOS-IT) : 3.11
Consensus Log Po/w : 2.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.56
Solubility : 0.404 mg/ml ; 0.00273 mol/l
Class : Soluble
Log S (Ali) : -2.33
Solubility : 0.697 mg/ml ; 0.0047 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.49
Solubility : 0.0483 mg/ml ; 0.000326 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 2142-71-4 ]

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

Application In Synthesis of [ 2142-71-4 ]

* 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 [ 2142-71-4 ]

[ 2142-71-4 ] Synthesis Path-Downstream   1~16

  • 2
  • [ 21900-46-9 ]
  • [ 506-82-1 ]
  • [ 2142-71-4 ]
  • 4
  • [ 64-19-7 ]
  • [ 603-79-2 ]
  • [ 2142-71-4 ]
  • 7
  • [ 33334-67-7 ]
  • [ 2142-71-4 ]
  • 8
  • [ 95-47-6 ]
  • [ 64-19-7 ]
  • [ 2142-71-4 ]
  • [ 3637-01-2 ]
  • 9
  • [ 2142-71-4 ]
  • [ 1576-35-8 ]
  • 2,3-dimethylacetophenone tosylhydrazone [ No CAS ]
  • 10
  • [ 69849-04-3 ]
  • Cr(CO)3(o-xylene) [ No CAS ]
  • [ 2142-71-4 ]
  • [ 3637-01-2 ]
  • 11
  • [ 87-59-2 ]
  • [ 2142-71-4 ]
  • 12
  • [ 2142-71-4 ]
  • 1-(2,3-dimethylphenyl)diazoethane [ No CAS ]
  • 13
  • [ 2142-71-4 ]
  • 2,3-dimethylacetophenone tosylhydrazone Na salt [ No CAS ]
  • 15
  • [ 2142-71-4 ]
  • [ 944267-28-1 ]
YieldReaction ConditionsOperation in experiment
-(Diethoxymethyl)imidazole (76.0 g, 446 mmol) and N,N,N,N-tetramethylethylene diamine (67.6 mL, 446 mmol) were dissolved in 2-methyltetrahydrofuran (400 ml) and cooled to -40 C., under nitrogen. n-Butyl lithium (2.5M in hexane, 180 ml, 446 mmol) was added slowly maintaining the reaction temperature at <-25 C. throughout. The reaction mixture was stirred for an hour and allowed to warm to 0 C., after which <strong>[2142-71-4]2,3-dimethylacetophenone</strong> (44.00 g, 297.00 mmol) was added whilst maintaining the reaction temperature at <15 C. throughout. The reaction was stirred at room temperature overnight and then quenched with aqueous hydrochloric acid (2N, 1 l). The mixture was extracted with ethyl acetate (500 ml) and to the aqueous layer was added sodium carbonate. The aqueous layer was further extracted with ethyl acetate (800 ml) and the combined extracts were washed with water (500 ml), dried (MgSO4) and concentrated in vacuo to give the title compound (48.9 g).Experimental MH+ 217.2; expected 217.1
  • 16
  • C14H20O [ No CAS ]
  • [ 2142-71-4 ]
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