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[ CAS No. 140695-84-7 ] {[proInfo.proName]}

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Chemical Structure| 140695-84-7
Chemical Structure| 140695-84-7
Structure of 140695-84-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 140695-84-7 ]

CAS No. :140695-84-7 MDL No. :MFCD02683203
Formula : C11H21NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :OJCLHERKFHHUTB-VIFPVBQESA-N
M.W : 215.29 Pubchem ID :1514448
Synonyms :

Calculated chemistry of [ 140695-84-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.56
TPSA : 49.77 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.65
Log Po/w (XLOGP3) : 1.17
Log Po/w (WLOGP) : 1.24
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : 0.93
Consensus Log Po/w : 1.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.65
Solubility : 4.84 mg/ml ; 0.0225 mol/l
Class : Very soluble
Log S (Ali) : -1.81
Solubility : 3.33 mg/ml ; 0.0155 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.11
Solubility : 16.7 mg/ml ; 0.0774 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.69

Safety of [ 140695-84-7 ]

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

Applications of [ 140695-84-7 ]

tert-Butyl (S)-3- (hydroxymethyl)piperidine-1-carboxylate (CAS: 140695-84-7) can be used in the preparation of GSK690693 (CAS: 937174-76-0). GSK690693 functions as an inhibitor of protein kinase B/AKT. It has the capability to hinder growth and prevent apoptosis in acute lymphoblastic leukemia cell lines.

Application In Synthesis of [ 140695-84-7 ]

* 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 [ 140695-84-7 ]

[ 140695-84-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 140695-84-7 ]
  • [ 140645-23-4 ]
YieldReaction ConditionsOperation in experiment
g)2) Analogously to e), f) and g)1), from t-butyl (S)-3-hydroxymethyl-1-piperidinecarboxylate there is obtained t-butyl (R)-3-aminomethyl-1-piperidinecarboxylate, [alpha]D25 =+23.0 (c=0.4, EtOH).
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