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[ CAS No. 109-08-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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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+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 109-08-0
Chemical Structure| 109-08-0
Structure of 109-08-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 109-08-0 ]

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Product Details of [ 109-08-0 ]

CAS No. :109-08-0 MDL No. :MFCD00006142
Formula : C5H6N2 Boiling Point : -
Linear Structure Formula :(C4H3N2)CH3 InChI Key :CAWHJQAVHZEVTJ-UHFFFAOYSA-N
M.W : 94.11 Pubchem ID :7976
Synonyms :

Calculated chemistry of [ 109-08-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 27.0
TPSA : 25.78 ?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) : -6.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.17
Log Po/w (XLOGP3) : 0.21
Log Po/w (WLOGP) : 0.78
Log Po/w (MLOGP) : -0.51
Log Po/w (SILICOS-IT) : 1.46
Consensus Log Po/w : 0.62

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.19
Solubility : 6.08 mg/ml ; 0.0646 mol/l
Class : Very soluble
Log S (Ali) : -0.31
Solubility : 46.0 mg/ml ; 0.489 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.95
Solubility : 1.06 mg/ml ; 0.0112 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 109-08-0 ]

Signal Word:Danger Class:3
Precautionary Statements:P261-P305+P351+P338 UN#:1993
Hazard Statements:H225-H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 109-08-0 ]

* 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.

  • Downstream synthetic route of [ 109-08-0 ]

[ 109-08-0 ] Synthesis Path-Downstream   1~14

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YieldReaction ConditionsOperation in experiment
39% 2-Methoxybenzonitrile (3.0 g, 22.5 mmol) and 2-methylpyrazine (2.2 g, 23.0 mmol) were dissolved in an ice-water bathIn dry tetrahydrofuran (50 mL) and stirred under nitrogen for 1.5 hours.under this conditionLithium diisopropylamide (23 mL, 45.06 mmol, tetrahydrofuran solution) was slowly added, and the addition was complete and the temperature was raised to 40C and stirring was continued for 3 hours.The reaction solution was cooled to ambient temperature, quenched with ammonium chloride solution, extracted with ethyl acetate (50 mL × 3), dried over anhydrous sodium sulfate, and filtered.The organic layer was concentrated under reduced pressure and the residue was purified by flash column chromatography (petroleum ether/ethyl acetate = 1/1) to give compound 5.1 as a yellow solid.Body (2.2 g, yield: 39%).
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  • [ 18433-97-1 ]
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