Home Cart Sign in  
Chemical Structure| 1198273-64-1 Chemical Structure| 1198273-64-1

Structure of 1198273-64-1

Chemical Structure| 1198273-64-1

*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 [ 1198273-64-1 ]

CAS No. :1198273-64-1
Formula : C13H20BrFOSi
M.W : 319.29
SMILES Code : C[Si](C(C)(C)C)(OCC1=C(F)C=CC=C1Br)C
MDL No. :MFCD33551388

Safety of [ 1198273-64-1 ]

Application In Synthesis of [ 1198273-64-1 ]

* 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 [ 1198273-64-1 ]

[ 1198273-64-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 261723-33-5 ]
  • [ 18162-48-6 ]
  • [ 1198273-64-1 ]
YieldReaction ConditionsOperation in experiment
With 1H-imidazole; In tetrahydrofuran; for 16h; 9.2(2-Bromo-6-fluorobenzyloxy)-tert-butyldimethylsilaneIn a 500 ml round-bottomed flask, 15.7 g (0.076 mol) of the compound obtained previously are dissolved in 230 ml of THF, and 7.8 g (0.115 mol) of imidazole are added, followed by 13.8 g (0.092 mol) of tert-butyldimethylsilane chloride, and the reaction mixture is stirred for 16 hours.The solvent is then evaporated off under reduced pressure, the residue is taken up between water and diethyl ether, the resulting product is separated by settling out, and the organic phase is washed with water and dried over sodium sulphate.After evaporation of the solvent, 25 g of oil are recovered.1H NMR (CDCl3, delta in ppm): 0.0 (s, 6H); 0.8 (s, 9H); 4.7 (s, 2H); from 6.8 to 7.05 (m, 2H); 7.25 (d, 1H).
With 1H-imidazole; In tetrahydrofuran; for 16h; 14.2 (2-Bromo-6-fluorobenzyloxy(tert-butyl)dimethylsilane15.7 g (0.076 mol) of the compound obtained above are dissolved in 230 ml of THF in a 500 ml round-bottomed flask, 7.8 g (0.115 mol) of imidazole and then 13.8 g (0.092 mol) of tert-butyldimethylchlorosilane are added and the reaction mixture is stirred for 16 hours.The solvent is then evaporated under reduced pressure, the residue is taken up between water and diethyl ether, separation by settling is carried out and the organic phase is washed with water and dried over sodium sulphate.After evaporating the solvent, 25 g of oil are collected.1H NMR (CDCl3, delta in ppm): 0.0 (s, 6H); 0.8 (s, 9H); 4.7 (s, 2H); from 6.8 to 7.05 (m, 2H); 7.25 (d, 1H).
 

Historical Records