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[ CAS No. 163765-44-4 ] {[proInfo.proName]}

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Chemical Structure| 163765-44-4
Chemical Structure| 163765-44-4
Structure of 163765-44-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 163765-44-4 ]

CAS No. :163765-44-4 MDL No. :MFCD02683205
Formula : C10H20N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FMLPQHJYUZTHQS-MRVPVSSYSA-N
M.W : 200.28 Pubchem ID :2756811
Synonyms :
Chemical Name :(R)-1-Boc-3-Methylpiperazine

Calculated chemistry of [ 163765-44-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 63.31
TPSA : 41.57 ?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) : -6.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.73
Log Po/w (XLOGP3) : 0.89
Log Po/w (WLOGP) : 0.45
Log Po/w (MLOGP) : 0.86
Log Po/w (SILICOS-IT) : 0.6
Consensus Log Po/w : 1.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.44
Solubility : 7.2 mg/ml ; 0.0359 mol/l
Class : Very soluble
Log S (Ali) : -1.35
Solubility : 8.99 mg/ml ; 0.0449 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.44
Solubility : 7.29 mg/ml ; 0.0364 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.72

Safety of [ 163765-44-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 163765-44-4 ]

* 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 [ 163765-44-4 ]

[ 163765-44-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 2895-21-8 ]
  • [ 163765-44-4 ]
  • C10H21N3O*2ClH [ No CAS ]
  • 2
  • [ 2895-21-8 ]
  • [ 163765-44-4 ]
  • C15H29N3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
711 mg With sodium carbonate; In acetonitrile; at 60℃; for 18h; (1) The compound 1 (500 mg), the compound 2 (677 mg) and sodium carbonate (529 mg) were suspended inacetonitrile (10 mL), and the reaction mixture was stirred for 18 hours at 60 C. The reaction mixture was cooled toroom temperature, and then diluted with ethyl acetate, washed with water and brine, and dried over anhydroussodium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silicagel column chromatography (eluent: ethyl acetate-methanol; gradient: 100:0-95:5) to give the compound 3 (711 mg)as a colorless solid.MS (APCI) 300 [M+H]+
  • 3
  • [ 902586-59-8 ]
  • [ 163765-44-4 ]
  • propyl (R)-4-(9-chloro-5,6,7,8-tetrahydroacridine-3-carbonyl)-3-methylpiperazine-1-carboxylate [ No CAS ]
  • 4
  • [ 902586-59-8 ]
  • [ 163765-44-4 ]
  • tert-butyl 4-(9-chloro-5,6,7,8-tetrahydroacridine-3-carbonyl)-3-methylpiperazine-1-carboxylate [ No CAS ]
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