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[ CAS No. 62848-20-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Inaccessible (Haz class 6.1), Domestic USD 80+
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Chemical Structure| 62848-20-8
Chemical Structure| 62848-20-8
Structure of 62848-20-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 62848-20-8 ]

CAS No. :62848-20-8 MDL No. :MFCD07787006
Formula : C5H11NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :BWRWNUQAQPAYCK-UHFFFAOYSA-N
M.W : 101.15 Pubchem ID :11355447
Synonyms :

Calculated chemistry of [ 62848-20-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.84
TPSA : 21.26 ?2

Pharmacokinetics

GI absorption : Low
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) : 1.72
Log Po/w (XLOGP3) : -0.15
Log Po/w (WLOGP) : -0.39
Log Po/w (MLOGP) : -0.16
Log Po/w (SILICOS-IT) : 0.85
Consensus Log Po/w : 0.37

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.31
Solubility : 49.9 mg/ml ; 0.494 mol/l
Class : Very soluble
Log S (Ali) : 0.16
Solubility : 146.0 mg/ml ; 1.44 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.86
Solubility : 13.9 mg/ml ; 0.138 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.45

Safety of [ 62848-20-8 ]

Signal Word:Danger Class:3
Precautionary Statements:P261-P305+P351+P338 UN#:1993
Hazard Statements:H225-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 62848-20-8 ]

* 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.

  • Downstream synthetic route of [ 62848-20-8 ]

[ 62848-20-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 136725-50-3 ]
  • [ 62848-20-8 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In water; The free base was obtained by neutralization of the salt residue with saturated sodium carbonate (5 mL), extraction with 9/1 dichloromethane/methanol (3 x 20 mL), drying (potassium carbonate), and concentration, followed by capturing the amine on a SCX column and eulting with 2M ammonia in methanol:3-Methoxypyrrolidine.
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