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[ CAS No. 42113-13-3 ] {[proInfo.proName]}

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Chemical Structure| 42113-13-3
Chemical Structure| 42113-13-3
Structure of 42113-13-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 42113-13-3 ]

CAS No. :42113-13-3 MDL No. :MFCD06203848
Formula : C9H10O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QBMHMOKIFSCFCX-UHFFFAOYSA-N
M.W : 166.17 Pubchem ID :11240684
Synonyms :

Calculated chemistry of [ 42113-13-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.71
TPSA : 46.53 ?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) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.05
Log Po/w (XLOGP3) : 1.12
Log Po/w (WLOGP) : 1.49
Log Po/w (MLOGP) : 1.64
Log Po/w (SILICOS-IT) : 1.68
Consensus Log Po/w : 1.59

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.81
Solubility : 2.55 mg/ml ; 0.0154 mol/l
Class : Very soluble
Log S (Ali) : -1.69
Solubility : 3.39 mg/ml ; 0.0204 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.28
Solubility : 0.876 mg/ml ; 0.00527 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.36

Safety of [ 42113-13-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P273-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335-H412 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 42113-13-3 ]

* 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 [ 42113-13-3 ]

[ 42113-13-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67-56-1 ]
  • [ 15777-70-5 ]
  • [ 42113-13-3 ]
  • 2
  • [ 42113-13-3 ]
  • [ 109431-87-0 ]
  • tert-butyl (S)-3-(4-(methoxycarbonyl)-2-methylphenoxy)pyrrolidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; for 1h; To a solution of methyl 4-hydroxy-3-methylbenzoate (0.30 g, 1.80 mmol), (R)- tert-butyl-3-hydroxypyrrolidine-1-carboxylate (0.34 g, 1.80 mmol), and triphenylphosphine (0.58 g, 2.20 mmol) in dry THF (15 mL) was added diisopropyl azodicarboxylate (0.44 g, 2.20 mmol) at 0 ^C. Then, the temperature was allowed to rise to room temperature and stir for another 1 h. Upon completion, the reaction was diluted with CH2Cl2 (150 mL), washed with NaOH (1M) (50 mL × 2) and brine (50 mL × 2), dried over Na2SO4, and concentrated to give the crude product. The residue was purified by column chromatography (silica gel, hexanes:acetone = 8:1 to 6:1) to yield 65 (0.45 g, 75% yield) as a white solid.1H NMR (500 MHz, CDCl3): δ ppm 7.71-7.68 (m, 2H), 6.64 (d, J = 8.5 Hz, 1H), 4.84-4.80 (m, 1H), 3.72 (s, 3H), 3.51-3.36 (m, 4H), 2.05 (s, 3H), 2.04-2.00 (m, 2H), 1.32 (s, 9H).13C NMR (125 MHz, CDCl3): δ ppm 166.87, 159.15, 154.61, 154.53, 132.44, 129.18, 127.59, 127.54, 122.47, 111.21, 79.53, 76.73, 75.91, 51.82, 51.76, 51.51, 44.27, 43.91, 31.72, 31.00, 28.55. MS (ESI) m/z = 336.2 [M + H]+.
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