Home Cart Sign in  
Chemical Structure| 496880-72-9 Chemical Structure| 496880-72-9

Structure of 496880-72-9

Chemical Structure| 496880-72-9

*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 [ 496880-72-9 ]

CAS No. :496880-72-9
Formula : C14H11FO
M.W : 214.24
SMILES Code : O=CC(C1=CC=C(F)C=C1)C2=CC=CC=C2
MDL No. :MFCD21775119

Safety of [ 496880-72-9 ]

Application In Synthesis of [ 496880-72-9 ]

* 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 [ 496880-72-9 ]

[ 496880-72-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 459-57-4 ]
  • benzyldimethylsulfonium hydrogensulfate [ No CAS ]
  • [ 496880-72-9 ]
  • [ 347-84-2 ]
  • 2
  • trans-2-(4-fluorophenyl)-3-phenyl oxirane [ No CAS ]
  • [ 496880-72-9 ]
  • [ 347-84-2 ]
YieldReaction ConditionsOperation in experiment
65%Chromat.; 7%Chromat. With bismuth(lll) trifluoromethanesulfonate; at 20℃; for 0.0833333h;Ionic liquid; Schlenk technique; Green chemistry; General procedure: The diaryl-epoxide (0.25 mmol) was added to Bi(OTf)3dissolvedin 1 mL of [BMIM][NTf2] in a small schlenk tube. The reaction wasperformed under sonication at ambient temperature and moni-tored by GC. After completion, the reaction mixture was extractedrepeatedly with diethyl ether. The combined organic extractwas washed with water, dried over MgSO4, and the solvent was evaporated under vacuum and the crude product was purified bycolumn chromatography with ethyl acetate/n-hexane (10-20%).
70%Chromat.; 30%Chromat. With C8H17N2O3S(1+)*CF3O3S(1-); In dichloromethane; at 20℃; for 0.0833333h;Ionic liquid; General procedure: The diaryl-epoxide (0.25 mmol) was added to a solution of 10mol% [BMIM(SO3H)][OTf] in 2 mL of dry DCM. The reaction mix-ture was stirred at room temperature and monitored by GC. Aftercompletion, the reaction was quenched by adding 5 mL of water.The two layers were separated and the aqueous layer was washedwith 2 × 5 mL of CH2Cl2. The combined organic layers were driedover MgSO4and the solvent was evaporated under vacuum andthe residue was purified by column chromatography with ethylacetate/n-hexane (10-20%).
  • 3
  • [ 459-57-4 ]
  • [ 496880-72-9 ]
  • [ 347-84-2 ]
 

Historical Records