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Chemical Structure| 918488-42-3 Chemical Structure| 918488-42-3

Structure of 918488-42-3

Chemical Structure| 918488-42-3

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Product Details of [ 918488-42-3 ]

CAS No. :918488-42-3
Formula : C9H6BrNO
M.W : 224.05
SMILES Code : OC1=C(Br)C2=C(C=NC=C2)C=C1
MDL No. :MFCD27932776
InChI Key :UAKCWZYJYLLDBJ-UHFFFAOYSA-N
Pubchem ID :136092895

Safety of [ 918488-42-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 918488-42-3 ]

* 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 [ 918488-42-3 ]

[ 918488-42-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7651-82-3 ]
  • [ 918488-42-3 ]
YieldReaction ConditionsOperation in experiment
88% 5-Bromoisoquinoline-6-ol (9)7.9 ml_ (19.18 g, 120 mmol) of bromine were added dropwise to a suspension of 17.42 g (120 mmol) of compound 7 in 250 mL of chloroform at room temperature. After stirring for 2 h ethyl acetate was added. The precipitate was filtered, washed with ethyl acetate and dried. Aqueous NaHCO3 solution was added carefully. The precipitate was filtered and washed with NaHCO3 solution until the filtrate had a pH of 8. Drying gave 23.78 g (88percent) of compound 9 as an off-white solid.1H-NMR (d6-DMSO): delta = 11.30 (1 H, s), 9.13 (1 H, s), 8.48 (1 H, d, J = 5.9 Hz), 8.02 (1 H, d, J= 8.8 Hz), 7.78 (1H, J = 5.9 Hz), 7.40 (1H, d, J = 8.8 Hz). MS: m/z = 224 (MH+).
88% 5-Bromoisoquinoline-6-ol (2); 7.9 mL (19.18 g, 120 mmol) of bromine were added dropwise to a suspension of 17.42 g (120 mmol) of <strong>[7651-82-3]6-hydroxy isoquinoline</strong> in 250 mL of chloroform at room temperature. After stirring for 2 h, ethyl acetate was added. The precipitate was filtered, washed with ethyl acetate and dried. Aqueous NaHCO3 solution was added carefully. The precipitate was filtered and washed with NaHCO3 solution until the filtrate had a pH of 8. Drying gave 23.78 g (88percent) of 2 as an off-white solid.1H-NMR (de-DMSO): delta = 11.30 (1 H, s), 9.13 (1 H, s), 8.48 (1 H, d, J = 5.9 Hz), 8.02 (1 H, d, J= 8.8 Hz), 7.78 (1 H, J = 5.9 Hz), 7.40 (1 H, d, J = 8.8 Hz). MS: m/z = 224 (MH+).
 

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