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[ CAS No. 114306-17-1 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 114306-17-1
Chemical Structure| 114306-17-1
Chemical Structure| 114306-17-1
Structure of 114306-17-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 114306-17-1 ]

CAS No. :114306-17-1 MDL No. :MFCD21603847
Formula : C10H8BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :LNTDPDLGBFTITA-UHFFFAOYSA-N
M.W : 254.08 Pubchem ID :69477591
Synonyms :

Calculated chemistry of [ 114306-17-1 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 57.5
TPSA : 42.09 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.08 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.1
Log Po/w (XLOGP3) : 2.49
Log Po/w (WLOGP) : 2.86
Log Po/w (MLOGP) : 2.08
Log Po/w (SILICOS-IT) : 3.02
Consensus Log Po/w : 2.51

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.33
Solubility : 0.119 mg/ml ; 0.00047 mol/l
Class : Soluble
Log S (Ali) : -3.02
Solubility : 0.243 mg/ml ; 0.000957 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.22
Solubility : 0.0155 mg/ml ; 0.0000608 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.97

Safety of [ 114306-17-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 114306-17-1 ]

* 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 [ 114306-17-1 ]
  • Downstream synthetic route of [ 114306-17-1 ]

[ 114306-17-1 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 64-19-7 ]
  • [ 372077-73-1 ]
  • [ 114306-17-1 ]
YieldReaction ConditionsOperation in experiment
254 mg at 90℃; for 3 h; Silver acetate (341 mg,2.04 mmol) was added to a solution of monomer 2 in acetic acid(8 mL). After stirring for 3 h at 90 C, the mixture was cooled toroom temperature and filtered. The filtrate was evaporated todryness under reduced pressure. The residue was chromatographedon silica gel with dichloromethane as eluent to affordproduct 3 (yield: 254 mg, 63.0percent). 1H NMR (CDCl3, 600 MHz): 7.97 (s,1H), 7.69 (d, 1H), 7.33 (d, 1H), 7.29 (m, 1H), 7.17 (m, 1H), 2.36 (s, 9H);13C NMR (CDCl3, 600 MHz): 168.65, 131.70, 129.82, 125.78, 121.61,120.14, 114.64, 113.17, 112.90, 20.93.
Reference: [1] Dyes and Pigments, 2016, vol. 125, p. 54 - 63
  • 2
  • [ 563-63-3 ]
  • [ 372077-73-1 ]
  • [ 114306-17-1 ]
Reference: [1] RSC Advances, 2018, vol. 8, # 27, p. 14747 - 14752
  • 3
  • [ 52415-29-9 ]
  • [ 114306-17-1 ]
Reference: [1] Dyes and Pigments, 2016, vol. 125, p. 54 - 63
[2] RSC Advances, 2018, vol. 8, # 27, p. 14747 - 14752
  • 4
  • [ 108996-91-4 ]
  • [ 114306-17-1 ]
Reference: [1] Pr.roy.Soc.<B>, 1958, vol. 148, p. 481,491,493
  • 5
  • [ 116436-10-3 ]
  • [ 114306-17-1 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1912, vol. 388, p. 34
  • 6
  • [ 20776-50-5 ]
  • [ 114306-17-1 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1912, vol. 388, p. 34
  • 7
  • [ 101861-53-4 ]
  • [ 114306-17-1 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1912, vol. 388, p. 34
  • 8
  • [ 244256-21-1 ]
  • [ 108-24-7 ]
  • [ 114306-17-1 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1912, vol. 388, p. 34
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