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[ CAS No. 74654-07-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 74654-07-2
Chemical Structure| 74654-07-2
Structure of 74654-07-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 74654-07-2 ]

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Product Details of [ 74654-07-2 ]

CAS No. :74654-07-2 MDL No. :MFCD17215909
Formula : C7H17NO3 Boiling Point : No data available
Linear Structure Formula :H2NCH2CH2OCH2CH2OCH2CH2OCH3 InChI Key :OKUWOEKJQRUMBW-UHFFFAOYSA-N
M.W : 163.21 Pubchem ID :3018531
Synonyms :
Chemical Name :2-(2-(2-Methoxyethoxy)ethoxy)ethanamine

Calculated chemistry of [ 74654-07-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 8
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.73
TPSA : 53.71 ?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) : -8.22 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.32
Log Po/w (XLOGP3) : -1.3
Log Po/w (WLOGP) : -0.38
Log Po/w (MLOGP) : -0.77
Log Po/w (SILICOS-IT) : 0.37
Consensus Log Po/w : 0.05

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.5
Solubility : 510.0 mg/ml ; 3.13 mol/l
Class : Highly soluble
Log S (Ali) : 0.67
Solubility : 763.0 mg/ml ; 4.68 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -1.55
Solubility : 4.61 mg/ml ; 0.0282 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.36

Safety of [ 74654-07-2 ]

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

Application In Synthesis of [ 74654-07-2 ]

* 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 [ 74654-07-2 ]

[ 74654-07-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 5926-51-2 ]
  • [ 74654-07-2 ]
  • [ 1442447-58-6 ]
  • 2
  • [ 207399-07-3 ]
  • [ 74654-07-2 ]
  • C43H60N3O3(1+)*I(1-) [ No CAS ]
  • 3
  • [ 74654-07-2 ]
  • [ 404844-11-7 ]
  • C31H36N6O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 120℃; for 1h;Microwave irradiation; General procedure: 4-(Chloromethyl)-N-(4-(methyl-3-(4-(pyridin-3-yl)pyrimidine-2-ylamino)phenyl)benzamide (129 mg, 0.3 mmol) and mPEGn-NH2 (1.50 mmol, n=3, 5, 7, 9) was reacted under microwave conditions at 120C for one hour. After cooling to room temperature, DCM (100 mL) was added to the reaction mixture. The resulting solution was extracted with 1M HCl (50 mL). The acidic aqueous phase was neutralized with sodium carbonate, and then extracted with DCM (100 mL×2). The organic phase was dried over Na2SO4 and the solvent removed under reduced pressure. The resulting residue was purified by column chromatography (biotage: DCM/CH3OH, CH3OH, 5-10%, 25 CV). The desired products were obtained in yields: 65-85%. mPEG3-N-Imatinib (compound la) NMR (500 MHz, CDCl3) delta 2.27 (s, 3H), 2.62 (br., 1H), 2.76 (t, 2H), 3.31 (s, 3H), 3.49 (m, 2H), 3.59 (m, 8H), 3.80 (s, 2H), 7.08 (s, 1H), 7.12 (m, 1H), 7.28 (m, IH), 7.30 (m, 3H), 7.79 (d, 2H), 8.42 (m, 2H), 8.51(d, 2H), 8.62 (d, 1H), 9.17 (s, 1H); LC-MS (m/z) calculated, 556.3, found, 557.3 [M+H]+.
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