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[ CAS No. 20637-09-6 ] {[proInfo.proName]}

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Chemical Structure| 20637-09-6
Chemical Structure| 20637-09-6
Structure of 20637-09-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20637-09-6 ]

CAS No. :20637-09-6 MDL No. :MFCD07366753
Formula : C11H15NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :CLKHQWJXESOLCJ-UHFFFAOYSA-N
M.W : 193.24 Pubchem ID :88628
Synonyms :

Calculated chemistry of [ 20637-09-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 56.33
TPSA : 52.32 ?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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.12
Log Po/w (XLOGP3) : 2.09
Log Po/w (WLOGP) : 1.77
Log Po/w (MLOGP) : 1.96
Log Po/w (SILICOS-IT) : 2.04
Consensus Log Po/w : 2.0

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.34
Solubility : 0.879 mg/ml ; 0.00455 mol/l
Class : Soluble
Log S (Ali) : -2.82
Solubility : 0.293 mg/ml ; 0.00152 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.33
Solubility : 0.09 mg/ml ; 0.000466 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.28

Safety of [ 20637-09-6 ]

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 [ 20637-09-6 ]

* 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 [ 20637-09-6 ]

[ 20637-09-6 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 75-21-8 ]
  • [ 20637-09-6 ]
  • [ 305-03-3 ]
  • 2
  • [ 20637-02-9 ]
  • [ 20637-09-6 ]
YieldReaction ConditionsOperation in experiment
88% With hydrogen;palladium on activated charcoal; In methanol; for 3h; b) Methyl 4-(4-aminophenyl)butanoateA suspension of methyl 4-(4-nitrophenyl)butanoate (3.05 g, 13.67 mmol) and Pd/C (1.0 g, 10percent Pd on activated C, 1.09 mmol) in MeOH (40 ml_) was stirred under H2 atmosphere (balloon) for 3 h. The reaction mixture was filtered through Celite (washing with EtOAc). Solvent was concentrated off, to furnish 2.33 g of methyl 4-(4-aminophenyl)butanoate (brown solid, yield: 88percent). It was submitted to next step without purification.1H NMR (CDCI3, 250 MHz) delta ppm: 6.96 (d, J = 8.5 Hz, 2H), 6.63 (d, J = 8.2 Hz, 2H), 3.66 (s, 3H), 2.55 (t, J = 7.6 Hz, 2H), 2.31 (t, J = 7.7 Hz, 2H), 1.90 (q, J = 7.6 Hz, 2H).
  • 3
  • [ 20637-09-6 ]
  • [ 75-56-9 ]
  • [ 55774-31-7 ]
  • 4
  • [ 20637-09-6 ]
  • [ 544-92-3 ]
  • [ 20637-03-0 ]
  • 6
  • [ 1943-83-5 ]
  • [ 20637-09-6 ]
  • [ 113849-33-5 ]
  • 7
  • [ 20637-09-6 ]
  • [ 55661-43-3 ]
  • methyl 4-3-nitroso>ureido>phenyl>butyrate [ No CAS ]
  • 8
  • [ 20637-09-6 ]
  • [ 1208-03-3 ]
  • 4-<γ-(methoxycarbonyl)propyl>-N-<p-<bis-(β'-chlorethyl)amino>>benzylideneaniline [ No CAS ]
  • 9
  • [ 20637-09-6 ]
  • [ 624-65-7 ]
  • [ 101248-43-5 ]
  • 10
  • [ 6552-57-4 ]
  • [ 20637-09-6 ]
  • C15H15(2)H8NO4 [ No CAS ]
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