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Chemical Structure| 1334167-35-9 Chemical Structure| 1334167-35-9

Structure of 1334167-35-9

Chemical Structure| 1334167-35-9

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Product Details of [ 1334167-35-9 ]

CAS No. :1334167-35-9
Formula : C7H5ClIN3
M.W : 293.49
SMILES Code : CC1=C(N2C(C(Cl)=NC=C2)=N1)I
MDL No. :MFCD22384935

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Application In Synthesis of [ 1334167-35-9 ]

* 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 [ 1334167-35-9 ]

[ 1334167-35-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 85333-43-3 ]
  • [ 1334167-35-9 ]
YieldReaction ConditionsOperation in experiment
97% With N-iodo-succinimide; acetic acid; In dichloromethane; at 0 - 20℃; for 16h; N-Iodosuccinimide (14.1 g, 62 mmol) was added to a stirred solution of intermediate 4 (9.58 g, 57 mmol) in a mixture of DCM and acetic acid at 0 C. The mixture was allowed to warm to RT and then stirred for 16 h. The mixture was diluted with further DCM and washed with a saturated solution of sodium carbonate and sodium thiosulfite. The organic layer was separated, dried (Na2S04), filtered and the solvents evaporated in vacuo. The crude product was precipitated from diisopropyl ether to yieldintermediate 25 (16 g, 97%) as a pale brown solid which was used in the next step without further purification.
97% With N-iodo-succinimide; acetic acid; In dichloromethane; at 0 - 20℃; for 16h; Example A25 3-Iodo-<strong>[85333-43-3]8-chloro-2-methyl-imidazo[1,2-a]pyrazine</strong> N-Iodosuccinimide (14.1 g, 62 mmol) was added to a stirred solution of intermediate 4 (9.58 g, 57 mmol) in a mixture of DCM and acetic acid at 0 C. The mixture was allowed to warm to RT and then stirred for 16 h. The mixture was diluted with further DCM and washed with a saturated solution of sodium carbonate and sodium thiosulfite. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was precipitated from diisopropyl ether to yield intermediate 25 (16 g, 97%) as a pale brown solid which was used in the next step without further purification.
97% With N-iodo-succinimide; acetic acid; In dichloromethane; at 0 - 20℃; for 16h; N-Iodosuccinimide (14.1 g, 62 mmol) was added to a stirred solution of intermediate 6 (9.58 g, 57 mmol) in a mixture of DCM and acetic acid at 0 C. The mixture was allowed to warm to RT and then stirred for 16 h. The mixture was diluted with further DCM and washed with a saturated solution of sodium carbonate and sodium thiosulfite. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was precipitated from diisopropyl ether to yield intermediate 7 (16 g, 97%) as a pale brown solid which was used in the next step without further purification.
With N-iodo-succinimide; In dichloromethane; acetic acid; at 0 - 20℃; for 16h; N-Iodosuccinimide (14.1 g, 62 mmol) was added to a stirred solution of intermediate 6(9.58 g, 57 mmol) in a mixture ofDCM and acetic acid at 0 C. The mixture was allowed to warm toRT and then stirred for 16 h. The mixture was diluted with further DCM and washed with a saturated solution of sodium carbonate and sodium thiosulfite.The organic layer was separated, dried (Na2S04), filtered and the solvents evaporatedin vacuo. The crude product was precipitated from diisopropyl ether to yieldintermediate 7 (16 g, 97%) as a pale brown solid which was used in the next step without further purification.

 

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