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[ CAS No. 5616-81-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 5616-81-9
Chemical Structure| 5616-81-9
Structure of 5616-81-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5616-81-9 ]

CAS No. :5616-81-9 MDL No. :MFCD05864597
Formula : C7H15NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 145.20 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 5616-81-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.89
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) : -6.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.17
Log Po/w (XLOGP3) : 0.7
Log Po/w (WLOGP) : 0.55
Log Po/w (MLOGP) : 0.75
Log Po/w (SILICOS-IT) : 0.48
Consensus Log Po/w : 0.93

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.92
Solubility : 17.6 mg/ml ; 0.121 mol/l
Class : Very soluble
Log S (Ali) : -1.08
Solubility : 12.0 mg/ml ; 0.0827 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.6
Solubility : 3.64 mg/ml ; 0.0251 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.33

Safety of [ 5616-81-9 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P261-P305+P351+P338 UN#:1993
Hazard Statements:H225-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5616-81-9 ]

* 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 [ 5616-81-9 ]

[ 5616-81-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15855-06-8 ]
  • [ 5616-81-9 ]
  • [ 1370448-71-7 ]
YieldReaction ConditionsOperation in experiment
A slurry of <strong>[15855-06-8]2-chloro-6-methoxyisonicotinic acid</strong> (100 mg, 0.53 mmol), sacrcosine tert- butyl ester (1 16 mg, (0.64 mmol), chloro(di-2-norborylphosphino)(2- dimethylaminomethylferrocen-1 yl)palladium (II) (9.8 mg, 0.02 mmol) and sodium tert- butoxide (128 mg, 1 .3 mmol) in p-dioxane (3 ml_) were stirred at 1 10C for 18 hr. The reaction mixture was cooled and the solvent removed in vacuo. The residue was diluted with water, pH adjusted to 4 with 1 N aqueous hydrochloric acid and extrated with ethyl acetate (3 x 10 ml_). The combined organic layer was dried over magnesium sulfate, filtered, concentrated in vacuo and the residue flashchromatographed (0-10% methanol/dichloromethane) to afford the title compound (60 mg) as a yellow solid, m/z = 297.5 (M+1 ).
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