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[ CAS No. 2363-16-8 ] {[proInfo.proName]}

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Chemical Structure| 2363-16-8
Chemical Structure| 2363-16-8
Structure of 2363-16-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2363-16-8 ]

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Product Details of [ 2363-16-8 ]

CAS No. :2363-16-8 MDL No. :MFCD00553089
Formula : C8H6BrNO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BNNDHGPPQZVKMX-UHFFFAOYSA-N
M.W : 260.04 Pubchem ID :2736829
Synonyms :

Calculated chemistry of [ 2363-16-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.24
TPSA : 72.12 ?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) : -5.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.83
Log Po/w (XLOGP3) : 2.7
Log Po/w (WLOGP) : 2.14
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 0.25
Consensus Log Po/w : 1.7

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 : 0.139 mg/ml ; 0.000534 mol/l
Class : Soluble
Log S (Ali) : -3.87
Solubility : 0.0353 mg/ml ; 0.000136 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.71
Solubility : 0.507 mg/ml ; 0.00195 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.96

Safety of [ 2363-16-8 ]

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

Application In Synthesis of [ 2363-16-8 ]

* 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 [ 2363-16-8 ]

[ 2363-16-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 109-11-5 ]
  • [ 2363-16-8 ]
  • [ 864296-47-9 ]
YieldReaction ConditionsOperation in experiment
100% With caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 95℃; for 16h; 1.00 g (3.85 mmol) methyl 4-bromo-3-nitro-benzoate are dissolved in 6 ml dioxane with 389 mg (3.85 mmol) <strong>[109-11-5]morpholin-3-one</strong> under a nitrogen atmosphere and 36.6 mg (40 μmol) tris-(dibenzylideneacetone)-dipalladium(0), 67.1 mg (116 μmol) xantphos and 1.75 g (5.38 mmol) caesium carbonate are added. Under a nitrogen atmosphere and with stirring, the reaction mixture is heated to 95 C. for 16 hours. Then it is filtered, the solution is evaporated down i. vac. and evaporated with ether. The residue is further reacted without any more purification. Yield: 1.31 g (quantitative). C12H12N2O6 (280.24) Mass spectrum: (M+H)+=281 Rf value: 0.47 (Reversed phase 8; methanol/5% sodium chloride solution=6:4)
  • 2
  • [ 850568-54-6 ]
  • [ 2363-16-8 ]
  • C19H19NO6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,4-dioxane; water; at 100℃; for 0.5h;Inert atmosphere; A mixture of the methyl ester (0.5 g, 1.9 mmol) in Dioxane, boronic acid (0.51 g,2.3 mmol) and a 2M aqueous solution of Na2CO3 was added to a 50 mL RB flaskand the flask was purged with N2 for 15 min. Pd(PPh3)4 (0.10 g, 0.09 mmol) wasadded and the reaction mixture was slowly heated up to 100 °C and stirred for 30 minutes. The reaction mixture was poured in ice water and extracted with EtOAc.The crude material was purified by flash column chromatography (silica gel,Silica Flash?-Silicycle) using EtOAc:Hexane (1:1) to give the product as an offwhitesolid which after characterization was used in the following steps GeneralProcedures B and C.
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