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[ CAS No. 52373-72-5 ] {[proInfo.proName]}

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Chemical Structure| 52373-72-5
Chemical Structure| 52373-72-5
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Product Details of [ 52373-72-5 ]

CAS No. :52373-72-5 MDL No. :MFCD00066527
Formula : C7H12O4 Boiling Point : -
Linear Structure Formula :- InChI Key :DOWWCCDWPKGNGX-RXMQYKEDSA-N
M.W : 160.17 Pubchem ID :853166
Synonyms :

Calculated chemistry of [ 52373-72-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.14
TPSA : 44.76 ?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) : -7.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.16
Log Po/w (XLOGP3) : 0.38
Log Po/w (WLOGP) : 0.31
Log Po/w (MLOGP) : -0.09
Log Po/w (SILICOS-IT) : 0.86
Consensus Log Po/w : 0.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.94
Solubility : 18.4 mg/ml ; 0.115 mol/l
Class : Very soluble
Log S (Ali) : -0.89
Solubility : 20.8 mg/ml ; 0.13 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.79
Solubility : 26.0 mg/ml ; 0.163 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.01

Safety of [ 52373-72-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H227-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 52373-72-5 ]

* 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 [ 52373-72-5 ]

[ 52373-72-5 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 52373-72-5 ]
  • [ 114746-70-2 ]
YieldReaction ConditionsOperation in experiment
97%
Stage #1: With lithium hydroxide; water In tetrahydrofuran at 0℃; for 1.16667 h;
Stage #2: With phosphoric acid In water
Preparation 29:; (R)-2, 2-Dimethyl-1, 3-dioxolane-4-carboxylic acid; To a solution of methyl- (R)-2, 2-dimethyl-1, 3-dioxolane-4-carboxylate (1.8 grams, 11.24 mmol) in THF (20 mL) was added an aqueous solution (20 mL) of lithium hydroxide monohydrate (0.71 grams, 16.9 mmol) drop wise over a period of 10 minutes at 0 °C and stirring was continued for another 1 hour. The reaction mixture was diluted with 50 mL of water and extracted with ethyl acetate (50 mL), which was discarded. Further, the aqueous layer was acidified with 10 M phosphorous acid (H3PO4) and the pH was brought to 2. The aqueous layer was then extracted with ethyl acetate (50 mL x 4) and the combined organic layers were washed with water and brine and dried over sodium sulfate. Removal of volatiles left 1.6 grams (97percent) of the title acid, which was used directly for the next step.
Reference: [1] Patent: WO2005/82892, 2005, A2, . Location in patent: Page/Page column 72-73
[2] Journal of Agricultural and Food Chemistry, 2010, vol. 58, # 10, p. 6458 - 6464
[3] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 12, p. 3231 - 3234
[4] Journal of the American Chemical Society, 1998, vol. 120, # 38, p. 9735 - 9747
[5] Tetrahedron Letters, 2004, vol. 45, # 39, p. 7371 - 7373
[6] Journal of Organic Chemistry, 2005, vol. 70, # 15, p. 6129 - 6132
  • 2
  • [ 52373-72-5 ]
  • [ 67-56-1 ]
  • [ 114746-70-2 ]
Reference: [1] Tetrahedron Asymmetry, 2001, vol. 12, # 4, p. 545 - 556
[2] Tetrahedron Asymmetry, 2001, vol. 12, # 4, p. 545 - 556
[3] Tetrahedron Asymmetry, 2001, vol. 12, # 4, p. 545 - 556
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