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[ CAS No. 23583-21-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 23583-21-3
Chemical Structure| 23583-21-3
Structure of 23583-21-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 23583-21-3 ]

CAS No. :23583-21-3 MDL No. :MFCD00085541
Formula : C12H17NO2 Boiling Point : -
Linear Structure Formula :C7H7NHC2H4CO2C2H5 InChI Key :HCTJHQFFNDLDPF-UHFFFAOYSA-N
M.W : 207.27 Pubchem ID :90196
Synonyms :

Calculated chemistry of [ 23583-21-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.42
Num. rotatable bonds : 7
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 59.53
TPSA : 38.33 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.82
Log Po/w (XLOGP3) : 1.48
Log Po/w (WLOGP) : 1.58
Log Po/w (MLOGP) : 1.98
Log Po/w (SILICOS-IT) : 2.36
Consensus Log Po/w : 2.04

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.89
Solubility : 2.66 mg/ml ; 0.0128 mol/l
Class : Very soluble
Log S (Ali) : -1.89
Solubility : 2.66 mg/ml ; 0.0128 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -4.15
Solubility : 0.0146 mg/ml ; 0.0000706 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 23583-21-3 ]

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

Application In Synthesis of [ 23583-21-3 ]

* 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 [ 23583-21-3 ]

[ 23583-21-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 64-17-5 ]
  • [ 100-46-9 ]
  • [ 140-88-5 ]
  • [ 23583-21-3 ]
  • [ 6938-07-4 ]
  • 2
  • [ 100-46-9 ]
  • [ 140-88-5 ]
  • [ 23583-21-3 ]
  • [ 6938-07-4 ]
YieldReaction ConditionsOperation in experiment
80%; 10% With aluminum oxide; In neat (no solvent); at 95℃; for 3.0h;Green chemistry; General procedure: The amine (7.5 mmol) and the Michael acceptor (5 mmol) in a molar ratio of 1.5:1 were refluxedwith stirring in the presence of acidic alumina (1 g, 200 mol%). Heating was performed using an oilbath and the reaction was followed by TLC and GC until completion. The reaction was then allowedto cool down to room temperature and filtered through a filter paper. The catalyst was rinsed withethyl acetate/hexane and then concentrated by rotary evaporation. The crude reaction mixture waspurified using a silica-filled chromatographic column using hexane/ethyl acetate as eluents. Usually,for aliphatic amines, the mono-adduct was eluted using 7:3, 6:4 or 5:5 hexane/ethyl acetate whilstfor aromatic ones the solvent mixture used was 8:2 hexane/ethyl acetate. The yields of the purifiedproducts were recorded and then IR and NMR spectroscopy and MS spectrometry were performed.
  • 3
  • [ 5928-51-8 ]
  • [ 23583-21-3 ]
  • [ 96103-41-2 ]
  • 4
  • [ 539-74-2 ]
  • [ 100-46-9 ]
  • [ 23583-21-3 ]
  • [ 6938-07-4 ]
  • 5
  • [ 23583-21-3 ]
  • [ 1067915-34-7 ]
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