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[ CAS No. 588703-29-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 588703-29-1
Chemical Structure| 588703-29-1
Structure of 588703-29-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 588703-29-1 ]

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Product Details of [ 588703-29-1 ]

CAS No. :588703-29-1 MDL No. :MFCD11977827
Formula : C10H8O3 Boiling Point : -
Linear Structure Formula :- InChI Key :GVDHNZDNWGZFLB-UHFFFAOYSA-N
M.W : 176.17 Pubchem ID :22481705
Synonyms :

Calculated chemistry of [ 588703-29-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.49
TPSA : 39.44 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.25
Log Po/w (XLOGP3) : 2.18
Log Po/w (WLOGP) : 2.22
Log Po/w (MLOGP) : 1.38
Log Po/w (SILICOS-IT) : 2.23
Consensus Log Po/w : 2.05

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.69
Solubility : 0.363 mg/ml ; 0.00206 mol/l
Class : Soluble
Log S (Ali) : -2.64
Solubility : 0.402 mg/ml ; 0.00228 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.36
Solubility : 0.0769 mg/ml ; 0.000437 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.23

Safety of [ 588703-29-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 588703-29-1 ]

* 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 [ 588703-29-1 ]

[ 588703-29-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 478169-68-5 ]
  • [ 588703-29-1 ]
  • 2
  • [ 478169-68-5 ]
  • [ 67-56-1 ]
  • [ 588703-29-1 ]
YieldReaction ConditionsOperation in experiment
70% Methyl 3-hydroxy-4-[(trimethylsilyl)ethynyl]benzoate (4.15 g, 16.7 mmol) is dissolved in MeOH (45 ml) and treated with DIA (2.34 ml, 16.7 mmol). Copper iodide (159 mg, 0.84 mmol) is added portion-wise and the reaction is heated at 75° C. for 3 h. DARCO (2 g) is added and the reaction is stirred at 95° C. for an additional 2 h, then overnight at RT. The reaction is filtered, concentrated to a brown oil and the crude material is chromatographed over 300 g slurry-packed silica gel, eluting with 10percent EtOAc/hexane. The appropriate fractions are collected and concentrated to afford 2.05 g (70percent) of methyl 1-benzofuran-6-carboxylate as an orange crystalline solid. 1H NMR (400 MHz, CDCl3) delta3.97, 6.84, 7.65, 7.78, 7.98, 8.22 ppm.
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