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[ CAS No. 98166-23-5 ] {[proInfo.proName]}

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Chemical Structure| 98166-23-5
Chemical Structure| 98166-23-5
Structure of 98166-23-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 98166-23-5 ]

CAS No. :98166-23-5 MDL No. :MFCD07186238
Formula : C5H6O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YYRYKNXDWXDXSN-UHFFFAOYSA-N
M.W : 98.10 Pubchem ID :4672596
Synonyms :

Calculated chemistry of [ 98166-23-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.4
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 24.85
TPSA : 26.3 ?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) : -6.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.25
Log Po/w (XLOGP3) : 0.03
Log Po/w (WLOGP) : 0.14
Log Po/w (MLOGP) : -0.42
Log Po/w (SILICOS-IT) : 1.24
Consensus Log Po/w : 0.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.47
Solubility : 33.5 mg/ml ; 0.341 mol/l
Class : Very soluble
Log S (Ali) : -0.13
Solubility : 72.0 mg/ml ; 0.733 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.35
Solubility : 44.1 mg/ml ; 0.45 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.41

Safety of [ 98166-23-5 ]

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

Application In Synthesis of [ 98166-23-5 ]

* 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.

  • Upstream synthesis route of [ 98166-23-5 ]

[ 98166-23-5 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 445378-38-1 ]
  • [ 98166-23-5 ]
YieldReaction ConditionsOperation in experiment
97% With Dess-Martin periodane In dichloromethane at 0 - 20℃; for 5 h; 3,6-Dihydro-2H-pyran-3-ol (2.44 g,24.37 mmol) was dissolved in DCM (100 mL) and cooled to 0 °C before slowly adding Dess-Martin periodinane (10.34 g, 24.37 mmol). The reaction was allowed to slowly warm to room temperature over 5 h. The reaction was then filtered through celite. After- 79 -ATI-2514175vl concentrating the filtrate, the crude material was purified on a 100G SNAP Biotage column (0-80percent ethyl acetate in hexane) to give 2H-pyran-3(6H)-one (2.33 g, 23.75 mmol, 97 percent yield) as a colorless oil; 1H NMR (400 MHz, CDC13) δ ppm 7.07 - 7.17 (m, 1H), 6.15 - 6.25 (m, 1H), 4.39 (t, J=2.54 Hz, 2H), 4.19 (s, 2H).
Reference: [1] Patent: WO2012/145569, 2012, A1, . Location in patent: Page/Page column 79; 80
[2] Angewandte Chemie - International Edition, 2005, vol. 44, # 33, p. 5306 - 5310
[3] Synlett, 2006, # 4, p. 621 - 623
[4] Patent: WO2014/134566, 2014, A2, . Location in patent: Paragraph 0547
  • 2
  • [ 78735-39-4 ]
  • [ 98166-23-5 ]
Reference: [1] Synlett, 2006, # 4, p. 621 - 623
[2] Angewandte Chemie - International Edition, 2005, vol. 44, # 33, p. 5306 - 5310
[3] Patent: WO2014/134566, 2014, A2,
  • 3
  • [ 497063-16-8 ]
  • [ 98166-23-5 ]
Reference: [1] Tetrahedron Letters, 2002, vol. 43, # 40, p. 7263 - 7266
[2] Tetrahedron, 2007, vol. 63, # 21, p. 4472 - 4490
  • 4
  • [ 98166-29-1 ]
  • [ 98166-23-5 ]
Reference: [1] Archiv der Pharmazie, 1985, vol. 318, # 6, p. 548 - 555
  • 5
  • [ 98-00-0 ]
  • [ 98166-23-5 ]
Reference: [1] Patent: WO2012/145569, 2012, A1,
  • 6
  • [ 35436-57-8 ]
  • [ 98166-23-5 ]
Reference: [1] Patent: WO2012/145569, 2012, A1,
  • 7
  • [ 329684-87-9 ]
  • [ 98166-23-5 ]
Reference: [1] Patent: WO2012/145569, 2012, A1,
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