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[ CAS No. 6298-03-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 6298-03-9
Chemical Structure| 6298-03-9
Structure of 6298-03-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6298-03-9 ]

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Product Details of [ 6298-03-9 ]

CAS No. :6298-03-9 MDL No. :MFCD00237142
Formula : C10H18N2O4 Boiling Point : -
Linear Structure Formula :- InChI Key :JMZPOGGPUVRZMI-QMMMGPOBSA-N
M.W : 230.26 Pubchem ID :6994019
Synonyms :
Chemical Name :H-Lys(Aloc)-OH

Calculated chemistry of [ 6298-03-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.6
Num. rotatable bonds : 10
Num. H-bond acceptors : 5.0
Num. H-bond donors : 3.0
Molar Refractivity : 58.66
TPSA : 101.65 ?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) : -8.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.58
Log Po/w (XLOGP3) : -1.21
Log Po/w (WLOGP) : 0.48
Log Po/w (MLOGP) : -1.99
Log Po/w (SILICOS-IT) : 0.19
Consensus Log Po/w : -0.19

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.15
Solubility : 329.0 mg/ml ; 1.43 mol/l
Class : Highly soluble
Log S (Ali) : -0.43
Solubility : 85.5 mg/ml ; 0.371 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.16
Solubility : 15.9 mg/ml ; 0.0689 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.67

Safety of [ 6298-03-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280 UN#:N/A
Hazard Statements:H317 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 6298-03-9 ]

* 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 [ 6298-03-9 ]

[ 6298-03-9 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 372-75-8 ]
  • [ 2937-50-0 ]
  • [ 6298-03-9 ]
YieldReaction ConditionsOperation in experiment
100%
Stage #1: With copper (II) carbonate hydroxide In water for 0.5 h; Reflux
Stage #2: With sodium carbonate In water at 0 - 20℃; for 12 h;
Stage #3: With thioacetamide In water at 50℃; for 3 h;
Step 5.
A solution of 58-7 (10 g, 68.4 mmol) and Cu(OH)2C03 (15.12 g, 68.4 mmol) in H20 (100 mL) was heated at reflux for 30 min. Solids formed during reflux were removed by filtration while hot. The filtrate was cooled to 0°C and was adjusted to pH 9 by addition of solid Na2C03 (1.0 g). AllocCl (10.8 mL, 102.6 mmol) was added dropwise, while the solution stirred at 0°C. During the addition, the reaction mixture was maintained at pH 9 by the addition of solid Na2C03 (20 g). The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The blue solid product formed during the reaction was collected by filtration in quantitative yield. The solid copper salt of Orn( Alloc) collected above was suspended in H20 (200 mL) and two equivalents of thioacetamide (6.511 g, 86.66 mmol) were added to. The alkaline suspension was stirred at 50°C for 3 h, during which time, the solid slowly dissolved. The solution was then acidified to pH 2 with 2M HC1 and was further boiled for 5 min. The precipitated CuS was removed by filtration. The filtrate was concentrated under vacuum to about 100 mL, at which point the product hydrochloride salt of Orn(Alloc) 58-8 precipitated as a white solid in quantitative yield.
Reference: [1] Patent: WO2015/95227, 2015, A2, . Location in patent: Page/Page column 168; 169
  • 2
  • [ 56-87-1 ]
  • [ 2937-50-0 ]
  • [ 6298-03-9 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2011, vol. 2, # 5, p. 348 - 352
  • 3
  • [ 104669-73-0 ]
  • [ 6298-03-9 ]
Reference: [1] Tetrahedron Letters, 1986, vol. 27, # 21, p. 2365 - 2368
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