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[ CAS No. 194788-10-8 ] {[proInfo.proName]}

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Chemical Structure| 194788-10-8
Chemical Structure| 194788-10-8
Structure of 194788-10-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 194788-10-8 ]

CAS No. :194788-10-8 MDL No. :MFCD08705859
Formula : C5H8O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ZSHGVMYLGGANKU-UHFFFAOYSA-N
M.W : 116.12 Pubchem ID :22640986
Synonyms :

Calculated chemistry of [ 194788-10-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 26.97
TPSA : 57.53 ?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) : -7.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.85
Log Po/w (XLOGP3) : -0.37
Log Po/w (WLOGP) : -0.16
Log Po/w (MLOGP) : -0.38
Log Po/w (SILICOS-IT) : -0.11
Consensus Log Po/w : -0.03

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -0.26
Solubility : 63.7 mg/ml ; 0.549 mol/l
Class : Very soluble
Log S (Ali) : -0.38
Solubility : 48.9 mg/ml ; 0.421 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.73
Solubility : 621.0 mg/ml ; 5.35 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.26

Safety of [ 194788-10-8 ]

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

Application In Synthesis of [ 194788-10-8 ]

* 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.

  • Upstream synthesis route of [ 194788-10-8 ]

[ 194788-10-8 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 480449-99-8 ]
  • [ 194788-10-8 ]
Reference: [1] Patent: EP1577301, 2005, A1, . Location in patent: Page/Page column 145
[2] Patent: US2005/20645, 2005, A1,
[3] Patent: EP1405852, 2004, A1, . Location in patent: Page 133
  • 2
  • [ 4934-99-0 ]
  • [ 194788-10-8 ]
YieldReaction ConditionsOperation in experiment
81% With lithium hydroxide monohydrate In tetrahydrofuran; water at 20℃; Methyl cis-3-hydroxycyclobutylcarboxylate prepared in Example 1 (273.3 g, 2.1 mol, 1 eq.) was dissolvedIn H2O/THF (1L/1.5L),Lithium hydroxide monohydrate (218.2 g, 5.2 mol, 2.5 eq.) was then added.Stir overnight at room temperatureWhen the reaction is complete, remove THF.Adjust pH = 4 ~ 5,Then the mixture was extracted with a 4:1 volume ratio of chloroform/isopropanol.Combine the organic phase,Dry and concentrate to get crude product.The crude product was beaten with ethyl acetate/n-heptane,An off-white solid (197.4 g, 1.7 mol) was obtained,For the final product,Yield 81percent,97percent purity
Reference: [1] Patent: CN107903161, 2018, A, . Location in patent: Paragraph 0033; 0034
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