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[ CAS No. 41038-40-8 ]

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Chemical Structure| 41038-40-8
Chemical Structure| 41038-40-8
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Product Details of [ 41038-40-8 ]

CAS No. :41038-40-8 MDL No. :MFCD08442838
Formula : C10H14O3 Boiling Point : -
Linear Structure Formula :- InChI Key :FOEBAVBMMWYLTA-UHFFFAOYSA-N
M.W :182.22 Pubchem ID :11805372
Synonyms :

Calculated chemistry of [ 41038-40-8 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.4
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.36
TPSA : 38.69 Ų

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) : -6.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.43
Log Po/w (XLOGP3) : 1.38
Log Po/w (WLOGP) : 1.43
Log Po/w (MLOGP) : 1.22
Log Po/w (SILICOS-IT) : 1.86
Consensus Log Po/w : 1.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.98
Solubility : 1.9 mg/ml ; 0.0104 mol/l
Class : Very soluble
Log S (Ali) : -1.8
Solubility : 2.92 mg/ml ; 0.016 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.51
Solubility : 0.559 mg/ml ; 0.00307 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.03

Safety of [ 41038-40-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 41038-40-8 ]

* 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 [ 41038-40-8 ]

[ 41038-40-8 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 41038-40-8 ]
  • [ 1201-38-3 ]
YieldReaction ConditionsOperation in experiment
90% With oxygen In toluene at 110℃; for 5 h; General procedure: A mixture of 1b (100 mg, 0.818 mmol), SS-Pd (918 mg, 0.04 mmol Pd) and 3 ml of toluene was purged with molecular oxygen and stirred at 110 °C for 5 h. The progress of reaction was monitored on TLC. After completion of reaction, the reaction was cooled, diluted with ethyl acetate and filtered through cotton bed. The combined organic layer was evaporated under reduced pressure and crude residue was purified by silica gel (mesh 60-120) column chromatography (Hexane/EtOH 95:5) afforded 2b as colorless liquid (94 mg, 96percent).
Reference: [1] Tetrahedron Letters, 2011, vol. 52, # 38, p. 4954 - 4956
[2] Catalysis Communications, 2012, vol. 20, p. 68 - 70
[3] Tetrahedron Letters, 2013, vol. 54, # 23, p. 2924 - 2928
  • 2
  • [ 67-56-1 ]
  • [ 41038-40-8 ]
  • [ 1201-38-3 ]
  • [ 64807-84-7 ]
  • [ 72205-70-0 ]
Reference: [1] Journal of Organic Chemistry, 1980, vol. 45, # 3, p. 369 - 378
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