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[ CAS No. 2760-35-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2760-35-2
Chemical Structure| 2760-35-2
Structure of 2760-35-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 2760-35-2 ]

CAS No. :2760-35-2 MDL No. :
Formula : C9H10BrNO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 228.09 Pubchem ID :-
Synonyms :

Safety of [ 2760-35-2 ]

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Application In Synthesis of [ 2760-35-2 ]

* 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 [ 2760-35-2 ]

[ 2760-35-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2760-35-2 ]
  • [ 96433-09-9 ]
  • [ 1265678-96-3 ]
  • 2
  • [ 2760-35-2 ]
  • [ 33513-42-7 ]
  • [ 113092-96-9 ]
YieldReaction ConditionsOperation in experiment
61% With trichlorophosphate at 20 - 85℃; for 4h; 178 Phosphorous oxychloride (3 mE, excess) was treated with DMF (650 uE, 8.7 mmol, 1.5 eq.) and the solution allowed to return to ambient temperature. N-propionyl208 4-bromoaniline (1.32 g, 5.8 mmol, 1 eq.) was added and themixture heated at 85° C. for 4 h. The hot mixture was pouredonto ice (100 g), stirred until melted, and the solids werecollected by filtration. Washing with water and drying invacuo gave clean 6-bromo-2-chioro-3-methylquinoline (914mg, 6 1%). This intermediate (250 mg, 1.0 mmol) and phenol(3 mmol, 3. eq.) were converted, via Methods 11,3, and 5, tocompound 210(118mg, 42%). [M-H]=278. 1 mlz. Activity:
Same Skeleton Products
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