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Chemical Structure| 5332-25-2 Chemical Structure| 5332-25-2
Chemical Structure| 5332-25-2

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6-Bromoquinoline is an important quinoline derivative, widely used in drug synthesis and materials science. Its bromine substitution makes it a valuable tool for developing antibacterial, antiviral, and anticancer drugs.

Synonyms: 6-Br-Quinoline

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Product Details of 6-Bromoquinoline

CAS No. :5332-25-2
Formula : C9H6BrN
M.W : 208.05
SMILES Code : C1=CC=C2C(=N1)C=CC(=C2)Br
Synonyms :
6-Br-Quinoline
MDL No. :MFCD00024023
InChI Key :IFIHYLCUKYCKRH-UHFFFAOYSA-N
Pubchem ID :79243

Safety of 6-Bromoquinoline

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of 6-Bromoquinoline

* 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 [ 5332-25-2 ]

[ 5332-25-2 ] Synthesis Path-Downstream   1~6

  • 3
  • [ 5332-25-2 ]
  • [ 381-98-6 ]
  • 6-[(E)-3,3,3-trifluoro-1-propen-1-yl]quinoline [ No CAS ]
  • 4
  • [ 5332-25-2 ]
  • [ 98-80-6 ]
  • [ 3894-25-5 ]
  • [ 861872-54-0 ]
YieldReaction ConditionsOperation in experiment
35 mg; 45 mg With ammonium peroxodisulfate; zinc trifluoromethanesulfonate; silver nitrate; In dichloromethane; water; at 20℃; for 4h; General procedure: Ammonium persulfate (3 equiv, 342 mg), phenylboronic acid (1.5 equiv, 91 mg), silver nitrate (0.2 equiv, 17 mg), and zinc trifluoromethanesulfonate (0.2 equiv, 36 mg) were combined ina 10 mL round bottom flask. A heterocycle (1 equiv, 0.5 mmol) was then added to the same flask and solvated with water (0.4 mL) and CH2Cl2 (1.6 mL). The resulting mixture was sonicated for 10 sec and placed on a stir plate to stir vigorously at room temperature for 4 h. The reaction was quenched with 28% ammonium hydroxide (2 mL), diluted with water (10 mL), and extracted with CH2Cl2 (3 x 10 mL). The organic layer was dried over sodium sulfate, filtered through cotton, and evaporated en vacuo. The products were purified by column chromatography (SiO2, 5-20% EtOAc/hexanes). Products 3b, 3c, and 3d required further purification by crystallization as the trifluoromethanesulfonic acid salts and recrystallization from THF/hexanes.
  • 5
  • [ 5332-25-2 ]
  • [ 1128-56-9 ]
  • C18H14N4 [ No CAS ]
  • 6
  • [ 5332-25-2 ]
  • [ 100-59-4 ]
  • [ 3894-25-5 ]
 

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