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[ CAS No. 885271-63-6 ] {[proInfo.proName]}

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Chemical Structure| 885271-63-6
Chemical Structure| 885271-63-6
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Product Details of [ 885271-63-6 ]

CAS No. :885271-63-6 MDL No. :MFCD03840642
Formula : C9H7BrN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :YRCSUTRLSRFUKC-UHFFFAOYSA-N
M.W : 255.07 Pubchem ID :24728204
Synonyms :

Safety of [ 885271-63-6 ]

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
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Application In Synthesis of [ 885271-63-6 ]

* 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 [ 885271-63-6 ]

[ 885271-63-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 192945-49-6 ]
  • [ 885271-63-6 ]
YieldReaction ConditionsOperation in experiment
69% With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20℃; for 1h; Compound 2a (1.0 g, 5.68 mmol) and KOH (1.28 g, 22.7 mmol) were dissolved in DMF (15 mL) as a suspension and NBS (2.0 g, 11.4 mmol) was added.And the mixture was stirred at room temperature for 1 hour.The reaction was poured into water and extracted with EtOAc (100 mL x 2).The organic phase was washed with a saturated aqueous sodium bicarbonate solution and saturated brine, dried over sodium sulfate and filtered.The organic phase was concentrated and purified by column chromatography (EtOAc / Pet. Ether, 1/100 to 1/5, v / v).Obtained as a light yellow solid product 2b (1.0 g, 69%).
With N-Bromosuccinimide; potassium hydroxide; In N,N-dimethyl-formamide; for 1h; To a solution of lH-<strong>[192945-49-6]indazole-4-carboxylic acid methyl ester</strong> (380 mg, 2.2 mmol) in DMF (5 mL) was added N-bromosuccinimide (nuBS) (976 mg, 4.32 mmol) and KOeta (485 mg, 8.64 mmol). After 1 hour, the reaction mixture was diluted with saturated aqueous ammonium chloride (20 mL) and extracted with ethyl acetate (3 x 20 mL). The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine (20 mL), dried over sodium sulfate and concentrated in vacuo to afford the title compound as a solid.
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