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[ CAS No. 98231-07-3 ] {[proInfo.proName]}

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Chemical Structure| 98231-07-3
Chemical Structure| 98231-07-3
Structure of 98231-07-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 98231-07-3 ]

CAS No. :98231-07-3 MDL No. :MFCD11111944
Formula : C8H14O4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CHNARWNKXNPXOU-UHFFFAOYSA-N
M.W : 174.19 Pubchem ID :10487446
Synonyms :

Calculated chemistry of [ 98231-07-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.95
TPSA : 44.76 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.18 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.43
Log Po/w (XLOGP3) : 0.26
Log Po/w (WLOGP) : 0.56
Log Po/w (MLOGP) : 0.24
Log Po/w (SILICOS-IT) : 0.84
Consensus Log Po/w : 0.86

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.82
Solubility : 26.4 mg/ml ; 0.151 mol/l
Class : Very soluble
Log S (Ali) : -0.76
Solubility : 30.2 mg/ml ; 0.173 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.07
Solubility : 14.7 mg/ml ; 0.0841 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.28

Safety of [ 98231-07-3 ]

Signal Word:Warning Class:
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 98231-07-3 ]

* 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 [ 98231-07-3 ]

[ 98231-07-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 198995-91-4 ]
  • [ 98231-07-3 ]
YieldReaction ConditionsOperation in experiment
72% With toluene-4-sulfonic acid; In toluene; for 10h;Heating / reflux; To a solution of <strong>[198995-91-4]3-oxocyclobutane carboxylic benzyl ester</strong> (613 mg, 3 mmol) in toluene (6 mL) were added methanol (1.2 mL) and p-toluenesulfonic acid monohydrate (57 mg, 0.3 mmol), and the mixture was heated to reflux for 10 hours. The reaction solution was concentrated, and then thereto was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate, dried over magnesium sulfate, and then filtered. The filtrate was evaporated and purified by silica gel column chromatography (n-hexane/ethyl acetate = 20/1 to 3/ 1) to give the titled compound (378 mg, 72%). 1H NMR (CDCl3, 400 MHz) delta 3.70 (s, 3H), 3.17 (s, 3H), 3.15 (s, 3H), 2.94-2.84 (m, 1H), 2.48-2.34 (m, 4H).
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