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[ CAS No. 59718-84-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 59718-84-2
Chemical Structure| 59718-84-2
Structure of 59718-84-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 59718-84-2 ]

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Product Citations

Product Details of [ 59718-84-2 ]

CAS No. :59718-84-2 MDL No. :MFCD03789583
Formula : C8H9NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CCQFKEITVOTHIW-UHFFFAOYSA-N
M.W : 151.16 Pubchem ID :12264487
Synonyms :

Calculated chemistry of [ 59718-84-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.48
TPSA : 39.19 ?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) : -6.23 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.83
Log Po/w (XLOGP3) : 1.4
Log Po/w (WLOGP) : 1.18
Log Po/w (MLOGP) : 0.66
Log Po/w (SILICOS-IT) : 1.64
Consensus Log Po/w : 1.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.93
Solubility : 1.77 mg/ml ; 0.0117 mol/l
Class : Very soluble
Log S (Ali) : -1.83
Solubility : 2.25 mg/ml ; 0.0149 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.47
Solubility : 0.512 mg/ml ; 0.00339 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 59718-84-2 ]

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

Application In Synthesis of [ 59718-84-2 ]

* 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 [ 59718-84-2 ]

[ 59718-84-2 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 59718-84-2 ]
  • [ 116986-09-5 ]
YieldReaction ConditionsOperation in experiment
80.6% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 90℃; for 16h;Inert atmosphere; A mixture of methyl 3-methylpicolinate (4.1 g, 27.1 mmol), NBS (5.8 g, 32.5 mmol), and AIBN (100 mg, 0.61 mmol) in carbon tetrachloride (55 mL) was stuffed at 90 C for 16 h under nitrogen. The mixture was filtered and concentrated before being purified by column chromatography to give the desired product (5.0 g, 80.6%). ?H NMR (400 MHz, CDC13, ): 8.67 (dd, J= 1.6, 4.6 Hz, 1 H), 7.91 (dd, J= 1.5, 7.9 Hz, 1 H), 7.48 (dd, J= 4.6, 7.9 Hz, 1 H), 4.95 (s, 2 H), 4.07 - 4.03 (m, 3 H). LCMS (mlz): 229.9 (M+1).
  • 2
  • [ 594-27-4 ]
  • [ 157865-84-4 ]
  • [ 59718-84-2 ]
  • 3
  • [ 59718-84-2 ]
  • (2S,3R)-3-Methyl-piperidine-2-carboxylic acid methyl ester; hydrochloride [ No CAS ]
  • 4
  • [ 67-56-1 ]
  • [ 1071068-55-7 ]
  • [ 59718-84-2 ]
  • 5
  • [ 583-61-9 ]
  • [ 67-56-1 ]
  • [ 55589-47-4 ]
  • [ 59718-84-2 ]
  • 8
  • [ 937782-76-8 ]
  • [ 59718-84-2 ]
  • methyl 2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-oxopropionate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In 1,2-dimethoxyethane; for 4h;Heating / reflux; 5 g quantity of methyl 3- [2- (3-benzyloxy-4-methoxy phenyl) oxazol-4-yl] propionate obtained in Reference Example 48 <n="118"/>and 3.2 g of <strong>[59718-84-2]methyl 3-methylpicolinate</strong> were dissolved in 150 ml of dimethoxyethane. While stirring the solution with ice cooling 1.2 g of sodium hydride was added thereto and further stirred. The reaction mixture was heated and refluxed for 4 hours. At the completion of the reaction, a saturated aqueous ammonium chloride solution was added to the mixture while stirring with ice cooling, and the mixture was further stirred. After stirring the reaction mixture for 30 minutes, water was added thereto and ethyl acetate extraction was performed. The organic layer was washed twice with water, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n- hexane: ethyl acetate = 2:1), thereby yielding 5.5 g of colorless oily substance methyl 2- [2- (3-benzyloxy-4-methoxyphenyl) oxazol-4- ylmethyl] -3- (3-methylpyridin-2-yl) -3-oxopropionate. 1H-NMR (CDCl3) δ: 8.49 (IH, dd, J = 4.8, 1.2 Hz), 7.59-7.28 (1OH, m), 6.91 (IH, d, J = 9.0 Hz), 5.23-5.16 (3H, m) , 3.91 (3H, s) , 3.65 (3H, s), 3.37-3.18 (2H,m,) 2.59 (3H, s)
  • 9
  • [ 874-24-8 ]
  • [ 59718-84-2 ]
  • 10
  • [ 62733-99-7 ]
  • [ 59718-84-2 ]
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