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[ CAS No. 77112-52-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 77112-52-8
Chemical Structure| 77112-52-8
Structure of 77112-52-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 77112-52-8 ]

CAS No. :77112-52-8 MDL No. :MFCD08460079
Formula : C9H9N3O2 Boiling Point : -
Linear Structure Formula :C7H4N3O(OC2H5) InChI Key :SWABYVXORFBBAT-UHFFFAOYSA-N
M.W : 191.19 Pubchem ID :11845418
Synonyms :

Calculated chemistry of [ 77112-52-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.07
TPSA : 56.49 ?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) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.12
Log Po/w (XLOGP3) : 1.24
Log Po/w (WLOGP) : 0.91
Log Po/w (MLOGP) : -0.2
Log Po/w (SILICOS-IT) : 0.57
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) : -2.08
Solubility : 1.57 mg/ml ; 0.00824 mol/l
Class : Soluble
Log S (Ali) : -2.02
Solubility : 1.81 mg/ml ; 0.00946 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.2
Solubility : 1.21 mg/ml ; 0.00635 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 77112-52-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H317-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 77112-52-8 ]

* 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 [ 77112-52-8 ]

[ 77112-52-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 77112-52-8 ]
  • [ 87597-27-1 ]
YieldReaction ConditionsOperation in experiment
With bromine; In ethanol; for 1.5h;Heating / reflux; To the suspension of imidazo[1,2-a]pyrazine-2-carboxylic acid ethyl ester (0.3 g, 0.0016 mol) in anhydrous ethanol (7 mL), the chilled solution of bromine (0.16 mL, 0.0032 mol) in anhydrous ethanol (7 mL) was added dropwise and the resulting mixture was heated at reflux under continuous nitrogen flow for 1.5 hours. The reaction mixture was concentrated under reduced pressure and treated with the saturated solution of sodium bicarbonate in water (50 mL). The aqueous layer was extracted with ethyl acetate (3x25 mL), the combined organic extracts were dried with magnesium sulfate and concentrated. The residue was suspended in heptane (30 mL) and the precipitate was collected by filtration and dried to yield 5-bromo- imidazo [1,2-a]pyrazine-2-carboxylic acid ethyl ester (0.075 g, 0.00028 mol) as a yellow solid. m/z: (M + H) + 270,272.
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