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[ CAS No. 196613-57-7 ] {[proInfo.proName]}

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Chemical Structure| 196613-57-7
Chemical Structure| 196613-57-7
Structure of 196613-57-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 196613-57-7 ]

CAS No. :196613-57-7 MDL No. :MFCD07371372
Formula : C11H22N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :YCOKHOLOSGJEGL-UHFFFAOYSA-N
M.W : 214.30 Pubchem ID :18946151
Synonyms :

Calculated chemistry of [ 196613-57-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 64.11
TPSA : 55.56 ?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) : -6.84 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.64
Log Po/w (XLOGP3) : 1.08
Log Po/w (WLOGP) : 1.35
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : 0.59
Consensus Log Po/w : 1.36

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 : 4.79 mg/ml ; 0.0223 mol/l
Class : Very soluble
Log S (Ali) : -1.84
Solubility : 3.11 mg/ml ; 0.0145 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.2
Solubility : 13.5 mg/ml ; 0.063 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.8

Safety of [ 196613-57-7 ]

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

Application In Synthesis of [ 196613-57-7 ]

* 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 [ 196613-57-7 ]

[ 196613-57-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4363-94-4 ]
  • [ 196613-57-7 ]
  • 4-[(6-methoxy-quinolin-4-ylmethyl)-amino]-azepane-1-carboxylic acid tert-butyl ester [ No CAS ]
  • 2
  • [ 196613-57-7 ]
  • [ 154012-15-4 ]
  • [ 1039738-26-5 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 90℃; for 0.5h;Microwave irradiation; Preparation 30 A mixture of <strong>[154012-15-4]ethyl 4,6-dichloro-5-nitronicotinate</strong> (3.05 g), racemic tert-butyl 4-aminoazepan-1-caboxylate (2.47 g), DIPEA (4 mL) and i-PrOH (7.625 mL) was stirred at 90C for 30 minutes under microwave irradiation. The reaction mixture was cooled to ambient temperature. The mixture was diluted with EtOAc (20 mL), and water (20 mL) was added. The organic layer was extracted, washed with brine, dried over anhydrous MgSO4, filtered. The filtrate was evaporated in vacuo. The residue was purified by silica gel column chromatography (EtOAc: n-hexane) to afford racemic tert-butyl 4-[2-chloro-5-(ethoxycarbonyl)-3-nitropyridine-4-yl]amino}azepan-1-carboxylate (3.43 g) as a yellow solid.
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