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[ CAS No. 519032-08-7 ] {[proInfo.proName]}

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Chemical Structure| 519032-08-7
Chemical Structure| 519032-08-7
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Product Details of [ 519032-08-7 ]

CAS No. :519032-08-7 MDL No. :MFCD12026362
Formula : C17H19N3O6 Boiling Point : -
Linear Structure Formula :- InChI Key :NIVUTAZNLHLBAN-UHFFFAOYSA-N
M.W : 361.35 Pubchem ID :135446261
Synonyms :

Calculated chemistry of [ 519032-08-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 26
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.29
Num. rotatable bonds : 8
Num. H-bond acceptors : 8.0
Num. H-bond donors : 3.0
Molar Refractivity : 90.4
TPSA : 130.87 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.75
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 1.58
Log Po/w (MLOGP) : 0.52
Log Po/w (SILICOS-IT) : 1.26
Consensus Log Po/w : 1.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.28
Solubility : 0.19 mg/ml ; 0.000525 mol/l
Class : Soluble
Log S (Ali) : -4.58
Solubility : 0.00945 mg/ml ; 0.0000262 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.02
Solubility : 0.0347 mg/ml ; 0.0000959 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 3.32

Safety of [ 519032-08-7 ]

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 [ 519032-08-7 ]

* 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.

  • Upstream synthesis route of [ 519032-08-7 ]

[ 519032-08-7 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 518047-98-8 ]
  • [ 762-42-5 ]
  • [ 519032-08-7 ]
YieldReaction ConditionsOperation in experiment
58%
Stage #1: at 20℃; for 2 h;
Stage #2: With xylene In methanol at 90 - 120℃; for 16 h; Inert atmosphere
Benzyl 2-amino-2-(hydroxyimino)-1,1-dimethylethylcarbamate (2.0 g, 8.0 mmol) was dissolved in 30 mL MeOH, dimethyl acetylenedicarboxylate (DMAD, 1.1 mL, 9.0 mmol) was added slowly. The mixture was stirred for 2 h at room temperature, and then concentrated under reduced pressure to give a white oil. The mixture of the oil and 80 mL xylene was stirred at 90 °C for 2 h and 120 °C for 2 h, then refluxed for 12 h under nitrogen, concentrated to yield the crude product. The crude product was recrystallized with 2 mL MeOH and 10 mL tert-butyl methyl ether to afford 5 as a yellow solid (1.7 g, 58 percent): 1H-NMR (DMSO-d6) δ: 7.35 (m, 5H), 5.00 (s, 2H), 3.83 (s, 3H), 1.48 (s, 6H); ESI-MS m/z 360 (M), 384 (M+Na) +.
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 23, p. 7114 - 7118
  • 2
  • [ 100134-82-5 ]
  • [ 519032-08-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2225 - 2239
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 23, p. 7114 - 7118
  • 3
  • [ 501-53-1 ]
  • [ 519032-08-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2225 - 2239
  • 4
  • [ 1064707-10-3 ]
  • [ 519032-08-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2008, vol. 51, # 18, p. 5843 - 5855
  • 5
  • [ 1064707-10-3 ]
  • [ 519032-08-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2225 - 2239
  • 6
  • [ 518047-98-8 ]
  • [ 519032-08-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2225 - 2239
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