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[ CAS No. 29274-22-4 ] {[proInfo.proName]}

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Chemical Structure| 29274-22-4
Chemical Structure| 29274-22-4
Structure of 29274-22-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 29274-22-4 ]

CAS No. :29274-22-4 MDL No. :MFCD04035685
Formula : C6H5N3O Boiling Point : -
Linear Structure Formula :- InChI Key :LSLIYLLMLAQRIS-UHFFFAOYSA-N
M.W : 135.12 Pubchem ID :135513288
Synonyms :

Calculated chemistry of [ 29274-22-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 35.01
TPSA : 50.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.24
Log Po/w (XLOGP3) : 0.3
Log Po/w (WLOGP) : 0.43
Log Po/w (MLOGP) : 0.39
Log Po/w (SILICOS-IT) : 0.04
Consensus Log Po/w : 0.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.53
Solubility : 3.96 mg/ml ; 0.0293 mol/l
Class : Very soluble
Log S (Ali) : -0.92
Solubility : 16.2 mg/ml ; 0.12 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.11
Solubility : 10.6 mg/ml ; 0.0783 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 29274-22-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 29274-22-4 ]

* 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 [ 29274-22-4 ]

[ 29274-22-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 1001-26-9 ]
  • [ 1225387-53-0 ]
  • [ 29274-22-4 ]
YieldReaction ConditionsOperation in experiment
99% With caesium carbonate; In N,N-dimethyl-formamide; at 110℃;Inert atmosphere; The compound 5-aminopyrazole (5 g, 60 mmol)And <strong>[1001-26-9]ethyl 3-ethoxyacrylate</strong> (13 g, 90 mmol)Cesium carbonate (29 g, 90 mmol)Was mixed in 100 ml of N, N-dimethylformamide,The reaction was heated to 110 ° C overnight.Cooled to room temperature, diluted with 200 ml of water,Ether extraction (40 mL x 3), the aqueous phase was concentrated under reduced pressure,The residue was purified by silica gel column chromatography (DCM: MeOH = 10: 1)4H-pyrazolo [1,5-a] pyrimidin-5-one (8 g) in 99percent yield.
  • 2
  • [ 29274-22-4 ]
  • [ 1224944-51-7 ]
  • 4
  • [ 29274-22-4 ]
  • [ 1224944-51-7 ]
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