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[ CAS No. 5339-26-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5339-26-4
Chemical Structure| 5339-26-4
Structure of 5339-26-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5339-26-4 ]

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Product Details of [ 5339-26-4 ]

CAS No. :5339-26-4 MDL No. :MFCD00007386
Formula : C8H8BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :NTURQZFFJDCTMZ-UHFFFAOYSA-N
M.W : 230.06 Pubchem ID :79266
Synonyms :

Calculated chemistry of [ 5339-26-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 52.91
TPSA : 45.82 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 2.9
Log Po/w (WLOGP) : 2.53
Log Po/w (MLOGP) : 2.81
Log Po/w (SILICOS-IT) : 0.99
Consensus Log Po/w : 2.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.27
Solubility : 0.125 mg/ml ; 0.000543 mol/l
Class : Soluble
Log S (Ali) : -3.52
Solubility : 0.069 mg/ml ; 0.0003 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.45
Solubility : 0.0822 mg/ml ; 0.000357 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.88

Safety of [ 5339-26-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H317-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 5339-26-4 ]

* 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 [ 5339-26-4 ]

[ 5339-26-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 295-64-7 ]
  • [ 5339-26-4 ]
  • [ 1879-55-6 ]
  • 1,4,7,10,13-pentaaza-1-N-(2-(4-nitrophenyl)ethyl)cyclopentadecane [ No CAS ]
  • 1,4-Bis-[2-(4-nitro-phenyl)-ethyl]-1,4,7,10,13-pentaaza-cyclopentadecane [ No CAS ]
  • 2
  • [ 858671-91-7 ]
  • [ 5339-26-4 ]
  • 2,5-bis[2-(4-nitrophenyl)ethyl]-2,5-diazabicyclo[2.2.2]octane [ No CAS ]
YieldReaction ConditionsOperation in experiment
To a flask charged with <strong>[858671-91-7]tert-butyl 2,5-diazabicyclo[2.2.2]octane-2-carboxylate</strong> (200 mg, 0.94 mmol) and a stir bar was added TFA (5 mL). The mixture was allowed to stir at RT for 2 hours. The volatiles were removed under reduced pressure. To the residue was added 1-(2-bromoethyl)-4-nitrobenzene (650 mg, 2.8 mmol), tetrabutylammonium iodide (35 mg, 0.094 mmol), K2CO3 (521 mg, 3.8 mmol), and DMF (5 mL). The mixture was heated to 80 C for 16 hours. LC showed formation of the desired product, which was separated by mass-directed HPLC. LC-MS (IE, m/z): 411 [M+1]+. (0.21 muM)
  • 3
  • [ 100-13-0 ]
  • [ 5339-26-4 ]
  • [ 19935-81-0 ]
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