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[ CAS No. 20511-15-3 ] {[proInfo.proName]}

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Chemical Structure| 20511-15-3
Chemical Structure| 20511-15-3
Structure of 20511-15-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20511-15-3 ]

CAS No. :20511-15-3 MDL No. :MFCD00235124
Formula : C5H5ClN2 Boiling Point : -
Linear Structure Formula :- InChI Key :GTLFLMZOABSJSV-UHFFFAOYSA-N
M.W : 128.56 Pubchem ID :581932
Synonyms :

Calculated chemistry of [ 20511-15-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.65
TPSA : 38.91 ?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) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.16
Log Po/w (XLOGP3) : 0.8
Log Po/w (WLOGP) : 1.33
Log Po/w (MLOGP) : 0.4
Log Po/w (SILICOS-IT) : 1.37
Consensus Log Po/w : 1.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.7
Solubility : 2.59 mg/ml ; 0.0201 mol/l
Class : Very soluble
Log S (Ali) : -1.2
Solubility : 8.14 mg/ml ; 0.0633 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.24
Solubility : 0.735 mg/ml ; 0.00571 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.25

Safety of [ 20511-15-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P337+P313-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 20511-15-3 ]

* 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 [ 20511-15-3 ]

[ 20511-15-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 20511-15-3 ]
  • [ 42926-52-3 ]
  • N-(4-chloropyridin-3-yl)-2-ethoxybenzamide [ No CAS ]
  • 2
  • [ 20511-15-3 ]
  • [ 42926-52-3 ]
  • 2-(2-ethoxyphenyl)thiazolo[4,5-c]pyridine [ No CAS ]
  • 3
  • [ 20511-15-3 ]
  • [ 1001-26-9 ]
  • C10H11ClN2O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
92% In toluene; for 0.25h;Reflux; In 250 ml two port in round bottomed flask, add 3 - amino -4 chloro pyridine (2.56 g, 20 mmol), dibutyl maleate (2.88 g, 20 mmol) and 100 ml toluene. The mixture in the argon atmosphere reflux stirring 15 minutes, cooling to room temperature, add 250 ml petroleum ether, produce a large amount of precipitation, filtration, drying, to obtain yellowish solid 4.16 g, yield 92percent.
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