Home Cart Sign in  
Chemical Structure| 1346498-59-6 Chemical Structure| 1346498-59-6

Structure of 1346498-59-6

Chemical Structure| 1346498-59-6

*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 [ 1346498-59-6 ]

CAS No. :1346498-59-6
Formula : C11H13FO3
M.W : 212.22
SMILES Code : O=C(OC)C1=CC=C(OC(C)C)C(F)=C1

Safety of [ 1346498-59-6 ]

Application In Synthesis of [ 1346498-59-6 ]

* 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 [ 1346498-59-6 ]

[ 1346498-59-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-30-9 ]
  • [ 403-01-0 ]
  • [ 1346498-59-6 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 1.5h; To <strong>[403-01-0]methyl 3-fluoro-4-hydroxy-benzoate</strong> (2.0 g, 11.8 mmol) in DMF (12 mL) was added K2CO3 (6.50 g, 47.04 mmol) followed by 2-iodopropane (2.35 mL, 23.5 mmol). The reaction mixture was heated at 60 °C for 1.5 hours. The reaction mixture was cooled and diluted with EtOAc, filtered and the solvent was evaporated in vacuo. The resulting residue was dissolved in EtOAc and washed sequentially with water (3 x 10 mL) and brine solution (1 x 10 mL). The organics were separated and dried over Na2SO4, filtered and concentrated in vacuo to give the desired ester. ESI-MS m/z calc. 212.2, found 213.3 (M+1)+; Retention time: 1.7 minutes (3 min run). 1H NMR (400 MHz, DMSO) delta 7.76 (ddd, J = 8.6, 2.1, 1.2 Hz, 1H), 7.69 (dd, J = 1 1.9, 2.1 Hz, 1H), 7.31 (t, J = 8.6 Hz, 1H), 4.79 (dt, J = 12.1, 6.0 Hz, 1H), 3.82 (s, 3H), 1.32 (d, J = 6.5 Hz, 6H).
 

Historical Records