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[ CAS No. 768371-16-0 ] {[proInfo.proName]}

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Chemical Structure| 768371-16-0
Chemical Structure| 768371-16-0
Structure of 768371-16-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 768371-16-0 ]

CAS No. :768371-16-0 MDL No. :MFCD01646390
Formula : C12H21NO5 Boiling Point : -
Linear Structure Formula :- InChI Key :WOCMUJFSDGAHNY-UHFFFAOYSA-N
M.W : 259.30 Pubchem ID :21064042
Synonyms :

Calculated chemistry of [ 768371-16-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 6
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 68.58
TPSA : 65.07 Ų

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) : -7.13 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.03
Log Po/w (XLOGP3) : 1.06
Log Po/w (WLOGP) : 0.8
Log Po/w (MLOGP) : 0.5
Log Po/w (SILICOS-IT) : 0.81
Consensus Log Po/w : 1.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.72
Solubility : 4.95 mg/ml ; 0.0191 mol/l
Class : Very soluble
Log S (Ali) : -2.02
Solubility : 2.49 mg/ml ; 0.0096 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.22
Solubility : 15.6 mg/ml ; 0.0603 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.39

Safety of [ 768371-16-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 768371-16-0 ]

* 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 [ 768371-16-0 ]

[ 768371-16-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 135072-32-1 ]
  • [ 768371-16-0 ]
YieldReaction ConditionsOperation in experiment
With 2,5-dihydrotoluene;palladium 10% on activated carbon; In ethanol; at 88℃; for 34h; A mixture of <strong>[135072-32-1]4-phenylmethyl-2-morpholinecarboxylic acid ethyl ester</strong> (J. Med. Chem. 1993, 36 (6), 683-9), (8.4 g, 32.4 MMOL), di-tert-butyl dicarbonate (8.47 g, 38.9 mmol), 1-methyl- 1, 4-CYCLOHEXADIENE (12.37 ML, 110 MMOL) and 10% palladium on charcoal (900 mg) in ethanol (330 ml) was heated to 88 C for 22 hours. TLC analysis showed starting material remaining, so the reaction was cooled, and additional 1-methyl-1, 4-cyclohexadiene (2.37 ml, 21 MMOL) and 10% palladium on charcoal (900 mg) were added, and the reaction mixture heated for a further 12 hours at 88 C. The cooled mixture was filtered through ARBOCELE and the filtrate evaporated under reduced pressure. The residual brown oil was purified by column chromatography on silica gel using an elution gradient of DICHLOROMETHANE : methanol (100: 0 to 95: 5) to give the title compound as a pale yellow oil, 5. 97 G. 'H NMR (400MHZ, CDCI3) : 8 1. 30 (t, 3H), 1.43 (s, 9H), 3.10 (m, 2H), 3.50-3. 70 (m, 2H), 4.01 (m, 1 H), 4.25 (q, 2H).
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