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[ CAS No. 314741-39-4 ] {[proInfo.proName]}

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Chemical Structure| 314741-39-4
Chemical Structure| 314741-39-4
Structure of 314741-39-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 314741-39-4 ]

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Product Details of [ 314741-39-4 ]

CAS No. :314741-39-4 MDL No. :MFCD04115326
Formula : C11H20N2O4 Boiling Point : -
Linear Structure Formula :- InChI Key :QUKAHFCVKNRRBU-QMMMGPOBSA-N
M.W : 244.29 Pubchem ID :1501855
Synonyms :

Calculated chemistry of [ 314741-39-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.82
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 69.4
TPSA : 67.87 ?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) : -7.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.64
Log Po/w (XLOGP3) : 0.41
Log Po/w (WLOGP) : -0.39
Log Po/w (MLOGP) : 0.22
Log Po/w (SILICOS-IT) : 0.11
Consensus Log Po/w : 0.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.28
Solubility : 12.7 mg/ml ; 0.0521 mol/l
Class : Very soluble
Log S (Ali) : -1.4
Solubility : 9.68 mg/ml ; 0.0396 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.13
Solubility : 18.2 mg/ml ; 0.0743 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.98

Safety of [ 314741-39-4 ]

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 [ 314741-39-4 ]

* 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 [ 314741-39-4 ]

[ 314741-39-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73841-32-4 ]
  • [ 314741-39-4 ]
  • (S)-1-tert-butyl 3-methyl 4-(3-iodopicolinoyl)piperazine-1,3-dicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With HATU; In dichloromethane; acetonitrile; at 20℃; for 12h; A solution of <strong>[73841-32-4]3-iodopicolinic acid</strong> 2a (1.8 g, 7.23 mmol), (S)-l-tert-butyl 3-methyl piperazine-1,3- dicarboxylate (1.766 g, 7.23 mmol), HATU (3.02 g, 7.95 mmol), DIEA (5.05 mL, 28.9 mmol) in DCM (100 mL) / Acetonitrile (20 mL) was stirred at r.t. for 12 h. DCM (50 mL) and satd. H4Cl (100 mL) were added. The DCM layer was washed with brine, dried over Na2S04, filtered and concentrated. The reaction was purified by column chromatography and the product was eluted by EtOAc to yield (S)-l-tert-butyl 3-methyl 4-(3-iodopicolinoyl)piperazine-l,3-dicarboxylate 2b.
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