Home Cart Sign in  
Chemical Structure| 209461-56-3 Chemical Structure| 209461-56-3

Structure of 209461-56-3

Chemical Structure| 209461-56-3

*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 [ 209461-56-3 ]

CAS No. :209461-56-3
Formula : C14H12O3
M.W : 228.24
SMILES Code : O=C(O)C1=CC=C(C)C(OC2=CC=CC=C2)=C1

Safety of [ 209461-56-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 209461-56-3 ]

* 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 [ 209461-56-3 ]

[ 209461-56-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5162-82-3 ]
  • [ 108-95-2 ]
  • [ 209461-56-3 ]
YieldReaction ConditionsOperation in experiment
39.8% With copper(l) iodide; copper; potassium carbonate; at 230℃; for 48h; To a solution of 68 (15.0 g, 87.9 mmol), 69 (77.3 mL, 87.9 mmol),Cu-powder (2.79 g, 43.9 mmol), CuI (8.37 g, 43.9 mmol) and K2CO3(24.3 g, 175 mmol) were mixed in a steel vessel and stirred for 2 days at230 C. Progress of the reaction mixture was monitored by TLC andLCMS. The resulting mixture was diluted with EtOAc (250 mL), 1 NNaOH (500 mL) and stirred for 1 h at room temperature. The aqueouslayer was extracted with EtOAc (3 × 250 mL) and then acidified with1 N HCl solution (pH 2) and extracted with EtOAc (3 × 250 mL). Theorganic layer was washed with brine solution (1 × 250 mL), dried withanhydrous sodium sulphate and then concentrated under vacuo to give58 (8.0 g, 39.8%) as a white solid. 1H NMR (400 MHz; DMSO-d6): 12.96(s, 1H), 7.64 (d, 1H), 7.46-7.38 (m, 3H), 7.30 (s, 1H), 7.15 (t, 1H), 6.97(d, 2H), 2.27 (s, 3H).
 

Historical Records