Home Cart 0 Sign in  

[ CAS No. 85-79-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 85-79-0
Chemical Structure| 85-79-0
Structure of 85-79-0 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 85-79-0 ]

Related Doc. of [ 85-79-0 ]

Alternatived Products of [ 85-79-0 ]

Product Details of [ 85-79-0 ]

CAS No. :85-79-0 MDL No. :MFCD00047595
Formula : C20H29N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :PUFQVTATUTYEAL-UHFFFAOYSA-N
M.W : 343.46 Pubchem ID :3025
Synonyms :
Cinchocaine;NSC 159055
Chemical Name :2-Butoxy-N-(2-(diethylamino)ethyl)quinoline-4-carboxamide

Calculated chemistry of [ 85-79-0 ]

Physicochemical Properties

Num. heavy atoms : 25
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.5
Num. rotatable bonds : 11
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 102.58
TPSA : 54.46 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.9
Log Po/w (XLOGP3) : 4.4
Log Po/w (WLOGP) : 3.49
Log Po/w (MLOGP) : 2.48
Log Po/w (SILICOS-IT) : 3.89
Consensus Log Po/w : 3.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.31
Solubility : 0.0168 mg/ml ; 0.0000488 mol/l
Class : Moderately soluble
Log S (Ali) : -5.26
Solubility : 0.00188 mg/ml ; 0.00000549 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -6.74
Solubility : 0.0000628 mg/ml ; 0.000000183 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.91

Safety of [ 85-79-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 85-79-0 ]

* 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.

  • Upstream synthesis route of [ 85-79-0 ]
  • Downstream synthetic route of [ 85-79-0 ]

[ 85-79-0 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 87864-14-0 ]
  • [ 71-36-3 ]
  • [ 85-79-0 ]
YieldReaction ConditionsOperation in experiment
96.4% With sodium hydroxide In hexaneReflux 150 g of 2-chloro-N-[2-(diethylamino)ethyl]-4-quinolinecarboxamide, 39 g of sodium hydroxide were added to 90 g of n-butanol,In a solution of 600 g of n-hexane, slowly raise the temperature to reflux and separate the water.After the water is divided, the temperature is lowered to room temperature, and deionized water is added for stirring for 1 hour, and the layering is static for 0.5 hour.The aqueous phase was separated by liquid separation, and the organic phase was further stirred by adding deionized water for 0.5 h. The aqueous phase was separated by liquid separation, and the organic phase was stirred and crystallized at 0 to 10 ° C for 8 hours.Filtration and drying gave 162.5 g of cinchine product, the molar yield was 96.4percent, and the liquid phase purity was 99.9percent.
Reference: [1] Patent: CN108003097, 2018, A, . Location in patent: Paragraph 0020-0022; 0023-0025; 0026-0028
  • 2
  • [ 98006-39-4 ]
  • [ 85-79-0 ]
Reference: [1] Patent: CH153033, 1930, ,
[2] Patent: GB368590, 1931, ,
  • 3
  • [ 2388-32-1 ]
  • [ 85-79-0 ]
Reference: [1] Patent: CH141231, 1927, ,
  • 4
  • [ 107779-36-2 ]
  • [ 100-36-7 ]
  • [ 85-79-0 ]
Reference: [1] Patent: CH141231, 1927, ,
[2] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 2741
Same Skeleton Products
Historical Records