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[ CAS No. 517-23-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 517-23-7
Chemical Structure| 517-23-7
Structure of 517-23-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 517-23-7 ]

CAS No. :517-23-7 MDL No. :MFCD00005394
Formula : C6H8O3 Boiling Point : No data available
Linear Structure Formula :C4H6O2C2H2O InChI Key :OMQHDIHZSDEIFH-UHFFFAOYSA-N
M.W : 128.13 Pubchem ID :10601
Synonyms :
Chemical Name :3-Acetyldihydrofuran-2(3H)-one

Calculated chemistry of [ 517-23-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 30.33
TPSA : 43.37 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.8
Log Po/w (XLOGP3) : 0.13
Log Po/w (WLOGP) : 0.14
Log Po/w (MLOGP) : -0.11
Log Po/w (SILICOS-IT) : 1.11
Consensus Log Po/w : 0.41

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.65
Solubility : 28.7 mg/ml ; 0.224 mol/l
Class : Very soluble
Log S (Ali) : -0.6
Solubility : 32.4 mg/ml ; 0.253 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.68
Solubility : 26.5 mg/ml ; 0.207 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.03

Safety of [ 517-23-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 517-23-7 ]

* 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 [ 517-23-7 ]

[ 517-23-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 517-23-7 ]
  • [ 17356-08-0 ]
  • [ 21585-16-0 ]
YieldReaction ConditionsOperation in experiment
56% To a solution of sodium (55.6 g, 2.4 mol) in ethanol (1000 ml) was added slowly 2-acetylbutyrolactone 155 g, 1.2 mol) after which thiourea (128 g, 1.65 mol) was added in small portions. The mixture was heated under reflux for 16 h, then concentrated, water (800 ml) was added and acidified slowly with concentrated hydrochloric acid (200 ml). The precipitate was collected and washed with water, isopropyl alcohol and petroleum ether. Yield 125 g (56%) of a white solid.
  • 2
  • [ 517-23-7 ]
  • [ 4922-98-9 ]
  • [ 74258-83-6 ]
  • 3
  • [ 517-23-7 ]
  • [ 10167-97-2 ]
  • [ 108-88-3 ]
  • 3-(2-chloroethyl)-7-methoxy-2-methyl-4H-pyrido[1,2-a]-pyrimidin-4-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
10 parts (30.4%) With ammonium hydroxide; trichlorophosphate; In hexane; ethyl acetate; a) A mixture of 17 parts of 5-methoxy-2-pyridinamine, 61 parts of phosphoryl chloride and 348 parts of methylbenzene was stirred for 2 hours at 60° C. 18 Parts of 3-acetyl-4,5-dihydro-2(3H)-furanone were added and the reaction mixture was stirred overnight at 90° C. The whole was poured into crushed ice and treated with ammonium hydroxide. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was stirred in a mixture of hexane and ethyl acetate (50:50 by volume). The precipitated product was filtered off and dried, yielding 10 parts (30.4percent) of 3-(2-chloroethyl)-7-methoxy-2-methyl-4H-pyrido-[1,2-a]pyrimidin-4-one; mp. 150° C. (intermediate 3)
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