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[ CAS No. 40987-24-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 40987-24-4
Chemical Structure| 40987-24-4
Structure of 40987-24-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 40987-24-4 ]

CAS No. :40987-24-4 MDL No. :MFCD02682009
Formula : C12H17NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :WQNIKIMRIXHNFF-UHFFFAOYSA-N
M.W : 207.27 Pubchem ID :2776358
Synonyms :

Calculated chemistry of [ 40987-24-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.39
TPSA : 32.7 ?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) : -7.02 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.46
Log Po/w (XLOGP3) : 0.77
Log Po/w (WLOGP) : 0.35
Log Po/w (MLOGP) : 0.86
Log Po/w (SILICOS-IT) : 1.72
Consensus Log Po/w : 1.23

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.71
Solubility : 4.06 mg/ml ; 0.0196 mol/l
Class : Very soluble
Log S (Ali) : -1.04
Solubility : 19.0 mg/ml ; 0.0918 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.59
Solubility : 0.529 mg/ml ; 0.00255 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.15

Safety of [ 40987-24-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 40987-24-4 ]

* 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 [ 40987-24-4 ]
  • Downstream synthetic route of [ 40987-24-4 ]

[ 40987-24-4 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 40987-25-5 ]
  • [ 40987-24-4 ]
YieldReaction ConditionsOperation in experiment
72%
Stage #1: at 215℃; for 3 h; Inert atmosphere
Stage #2: at 50℃; for 2 h; Reflux
Step 3b: Synthesis of (4-benzylmorpholin-2-yl)methanol 20.3 g of 4-benzyl-2-chloromethylmorpholine, previously obtained, 3.5 ml of water and then 45 ml of formamide (75-12-7) are placed in a 250 ml round-bottomed flask with a condenser and a thermometer and under argon. The reaction medium is heated at 215° C. at the reflux of formamide for 3 h and then cooled to 50° C. with a bath of ice-cold water. A further 3.5 ml of water are added and the refluxing is resumed for a further 2 h. After returning to ambient temperature (20° C.), the medium is poured into ice-cold water (150 ml), the resulting mixture is basified with 10M sodium hydroxide (50 ml) at pH=12, extraction is carried out twice with toluene, and the organic phases are combined and washed with a saturated NaCl solution (50 ml), dried over magnesium sulfate and brought to dryness under a vacuum of 3 mbar for 1 h. (4-Benzylmorpholin-2-yl)methanol (13.4 g) is isolated in the form of an amber oil (yield=72percent).
Reference: [1] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244
[2] Patent: US2013/274253, 2013, A1, . Location in patent: Paragraph 1825-1826
[3] Synthetic Communications, 1980, vol. 10, # 1, p. 59 - 74
  • 2
  • [ 769087-80-1 ]
  • [ 40987-24-4 ]
Reference: [1] Patent: US2010/63022, 2010, A1, . Location in patent: Page/Page column 29
  • 3
  • [ 174560-84-0 ]
  • [ 943443-03-6 ]
  • [ 40987-24-4 ]
Reference: [1] Journal of Organic Chemistry, 2008, vol. 73, # 9, p. 3662 - 3665
  • 4
  • [ 61636-32-6 ]
  • [ 40987-24-4 ]
Reference: [1] Journal of Chemical Research, Miniprint, 1999, # 3, p. 1001 - 1047
  • 5
  • [ 174560-84-0 ]
  • [ 40987-24-4 ]
Reference: [1] Synthetic Communications, 1980, vol. 10, # 1, p. 59 - 74
[2] Patent: US2013/274253, 2013, A1,
  • 6
  • [ 104-63-2 ]
  • [ 40987-24-4 ]
Reference: [1] Synthetic Communications, 1980, vol. 10, # 1, p. 59 - 74
[2] Patent: US2013/274253, 2013, A1,
  • 7
  • [ 40987-24-4 ]
  • [ 103003-01-6 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1985, vol. 33, # 9, p. 3766 - 3774
[2] Journal of Medicinal Chemistry, 1994, vol. 37, # 17, p. 2791 - 2796
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244
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