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[ CAS No. 1256823-49-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1256823-49-0
Chemical Structure| 1256823-49-0
Structure of 1256823-49-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1256823-49-0 ]

CAS No. :1256823-49-0 MDL No. :MFCD17014981
Formula : C7H8BrNO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 202.05 Pubchem ID :-
Synonyms :

Safety of [ 1256823-49-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1256823-49-0 ]

* 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 [ 1256823-49-0 ]

[ 1256823-49-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 186593-45-3 ]
  • [ 74-88-4 ]
  • [ 1256823-49-0 ]
YieldReaction ConditionsOperation in experiment
47% With potassium carbonate In N,N-dimethyl-formamide at 20℃; 15.I Part I - Synthesis of 3 -Bromo-5-methoxy-2-methylpyridine Into a 100-mL round-bottom flask, was placed a solution of 5-bromo-6-methylpyridin-3-ol (3 g, 16 mmol) in N.N-dimethylformamide (30 mL). Potassium carbonate (3.3 g, 24 mmol) was added, followed by iodomethane (3.4 g, 24 mmol). The mixture was stirred at room temperature overnight then diluted with ethyl acetate (100 mL), washed with water (3 x 100 mL), dried over anhydrous sodium sulfate, and concentrated. The residue was purified on a silica gel column eluting with petroleum ether/ethyl acetate (4: 1) to yield 3- bromo-5-methoxy-2-methylpyridine (1.5 g, 47%).
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