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[ CAS No. 86-59-9 ] {[proInfo.proName]}

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Chemical Structure| 86-59-9
Chemical Structure| 86-59-9
Structure of 86-59-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 86-59-9 ]

CAS No. :86-59-9 MDL No. :MFCD00047619
Formula : C10H7NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QRDZFPUVLYEQTA-UHFFFAOYSA-N
M.W : 173.17 Pubchem ID :66582
Synonyms :
Chemical Name :Quinoline-8-carboxylic acid

Calculated chemistry of [ 86-59-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.7
TPSA : 50.19 ?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) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.25
Log Po/w (XLOGP3) : 2.0
Log Po/w (WLOGP) : 1.93
Log Po/w (MLOGP) : 1.34
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 1.67

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.68
Solubility : 0.364 mg/ml ; 0.0021 mol/l
Class : Soluble
Log S (Ali) : -2.68
Solubility : 0.361 mg/ml ; 0.00209 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.07
Solubility : 0.147 mg/ml ; 0.000851 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 86-59-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 86-59-9 ]

* 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 [ 86-59-9 ]

[ 86-59-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 86-59-9 ]
  • [ 162167-97-7 ]
  • 3-[(quinoline-8-carbonyl)-amino]-methyl}-piperidine-1-carboxylic acid <i>tert</i>-butyl ester [ No CAS ]
  • 2
  • [ 6154-04-7 ]
  • [ 86-59-9 ]
  • [ 530-62-1 ]
  • 8-(2-methyl-1H-tetrazol-5-ylcarbamoyl)quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In water; N,N-dimethyl-formamide; Using the method of Example 12 the following compounds of the invention are prepared from the starting quinolines listed in the table. example 11 to a solution of 1.7 g. (10 mmole) of 8-quinoline carboxylic acid in 50 ml. of N,N-dimethylformamide is added 1.6 g. (10 mmole) of carbonyl diimidazole, and the mixture is stirred for four hours at 100 C. The reactive intermediate which is formed is reacted with 1.0 g. (10 mmole) of 5-amino-2-methyltetrazole. The reaction is carried out by adding the solution and two drops of trifluoroacetic acid to the stirred solution of reactive intermediate and heating for four hours at 140-150 C. The solution is then evaporated to remove the N,N-dimethylformamide. Water is added to the residue, the mixture is cooled, then filtered. The solid product is recrystallized from ethanol to provide 8-(2-methyl-1H-tetrazol-5-ylcarbamoyl)quinoline, m.p. 222-223 C.
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