Home Cart Sign in  
Chemical Structure| 882427-72-7 Chemical Structure| 882427-72-7

Structure of 882427-72-7

Chemical Structure| 882427-72-7

*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 [ 882427-72-7 ]

CAS No. :882427-72-7
Formula : C28H24O4
M.W : 424.49
SMILES Code : O=C(OCC1=CC=CC=C1)C2=CC=C(OCC3=CC=CC=C3)C(OCC4=CC=CC=C4)=C2

Safety of [ 882427-72-7 ]

Application In Synthesis of [ 882427-72-7 ]

* 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 [ 882427-72-7 ]

[ 882427-72-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 882427-72-7 ]
  • [ 1570-05-4 ]
YieldReaction ConditionsOperation in experiment
2.81 g General procedure: A solution of hydroxy benzoic acid (1.0 equiv), BnBr (3-5 equiv) and K2CO3 (10-15 equiv) in DMF was stirred overnight under argon. After filtration, the solution was concentrated in vacuo to afford the crude product. The crude product was dissolved in methanol and an aqueous solution of NaOH (75 equiv) was added. The mixture was stirred at room temperature overnight and the solution concentrated in vacuo to remove the methanol. The residue was acidified with 10 percent HCl to pH 2 and then partitioned between ethyl acetate and water. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by recrystallization from CH2CH2 / MeOH.
With water; potassium hydroxide; In ethanol; at 20 - 70℃; Take 1.5g (3.53mmol) compound 16a in 50mL round bottom flask, was added 20mL of ethanol, taking 1g (17.85mmol) of potassium hydroxide was dissolved in 10mL of water and slowly added to the flask and the reaction stirred until the reaction mixture was homogeneous at 70 status.The reaction mixture was evaporated to an excess of ethanol, add 100mL water, cooled to room temperature.4mol·L-1 was added dropwise to acidified till no white precipitate (pH3 ~ 4), filtered, washed with water, suction filtered and dried to give a white solid.
 

Historical Records

Technical Information

Categories