Home Cart Sign in  
Chemical Structure| 22019-50-7 Chemical Structure| 22019-50-7

Structure of 22019-50-7

Chemical Structure| 22019-50-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 22019-50-7 ]

CAS No. :22019-50-7
Formula : C9H8BrNO3
M.W : 258.07
SMILES Code : O=[N+](C1=CC(C(CBr)=O)=CC=C1C)[O-]
MDL No. :MFCD03964203

Safety of [ 22019-50-7 ]

Application In Synthesis of [ 22019-50-7 ]

* 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 [ 22019-50-7 ]

[ 22019-50-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50840-23-8 ]
  • [ 22019-50-7 ]
  • 6-methyl-2-(4-methyl-3-nitrophenyl)imidazo[1,2-a]pyrimidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
30% In ethanol;Reflux; 2-Bromo-l-(4-methyl-3-nitrophenyl)ethanone (300 mg, 1.16) and 2-amino-5- methylpyrimidine (200 mg, 1.83 mmol) were dissolved in EtOH (10 mL) and the solution refluxed overnight. The solution was diluted with DCM and washed with NaHC03 solution. The organic layer was concentrated and the residue purified by column chromatography to give the title compound (102 mg, yield 30%) as a yellow solid. MS m/z 269.9 [M+H]+.
30% In ethanol;Reflux; 2-Bromo-l-(4-methyi-3-mtroplienyi)ethanone (300 mg, 1.16) and 2-amino-5- methylpyrimidme (200 mg, 1.83 mmol) were dissolved in EtOH (10 mL) and the solution refluxed overnight. The solution was diluted with DCM and washed with NaHCCT solution The organic layer was concentrated and the residue purified by column chromatography to give the title compound (102 mg, yield 30%) as a yellow solid. MS m/z 269.9 [M+H jL
 

Historical Records

Technical Information

Categories