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[ CAS No. 127828-22-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 127828-22-2
Chemical Structure| 127828-22-2
Structure of 127828-22-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 127828-22-2 ]

CAS No. :127828-22-2 MDL No. :MFCD12031501
Formula : C9H20N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :VULKFBHOEKTQSF-UHFFFAOYSA-N
M.W : 204.27 Pubchem ID :12106198
Synonyms :
Chemical Name :tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate

Calculated chemistry of [ 127828-22-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.89
Num. rotatable bonds : 8
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 53.68
TPSA : 73.58 ?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) : -7.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.44
Log Po/w (XLOGP3) : -0.16
Log Po/w (WLOGP) : 0.49
Log Po/w (MLOGP) : 0.12
Log Po/w (SILICOS-IT) : 0.17
Consensus Log Po/w : 0.61

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.48
Solubility : 68.0 mg/ml ; 0.333 mol/l
Class : Very soluble
Log S (Ali) : -0.93
Solubility : 24.0 mg/ml ; 0.117 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.84
Solubility : 2.97 mg/ml ; 0.0145 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.59

Safety of [ 127828-22-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 127828-22-2 ]

* 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 [ 127828-22-2 ]

[ 127828-22-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42017-89-0 ]
  • [ 127828-22-2 ]
  • [ 1286173-97-4 ]
YieldReaction ConditionsOperation in experiment
35% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20℃; for 18h; tert-Butyl 2-(2-aminoethoxy)ethylcarbamate (300 mg, 1.47 mmol) was taken up in CH2Cl2 (15 mL) along with <strong>[42017-89-0]2-(4-(4-chlorobenzoyl)phenoxy)-2-methylpropanoic acid</strong> (<strong>[42017-89-0]fenofibric acid</strong>, 467 mg, 1.47 mmol) and EDCI (310 mg, 1.47 mmol). The resulting reaction mixture was stirred at room temperature for 18 h. It was then brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (9:1 CH2Cl2/MeOH) to afford tert-butyl 2-(2-(2-(4-(4-chlorobenzoyl)phenoxy)-2-methylpropanamido)ethoxy)ethylcarbamate (260 mg, 35%).
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