Home Cart Sign in  
Chemical Structure| 179803-79-3 Chemical Structure| 179803-79-3

Structure of 179803-79-3

Chemical Structure| 179803-79-3

*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 [ 179803-79-3 ]

CAS No. :179803-79-3
Formula : C26H18O2
M.W : 362.42
SMILES Code : OC1=CC=C(C2=C3C=CC=CC3=C(C4=CC=C(O)C=C4)C5=CC=CC=C25)C=C1
InChI Key :OPKQAOBTBQLNCB-UHFFFAOYSA-N
Pubchem ID :374566

Safety of [ 179803-79-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 179803-79-3 ]

* 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 [ 179803-79-3 ]

[ 179803-79-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 83883-26-5 ]
  • [ 179803-79-3 ]
  • C58H54O10 [ No CAS ]
YieldReaction ConditionsOperation in experiment
56.3% (0339) A 300 ml four-neck flask was charged with mesyl chloride (0.22 g, 0.00192 mol) and THF (7.29 g). In a nitrogen atmosphere at ?30° C., a solution of TEA (0.19 g, 0.00192 mol) and 4-(6-acryloxy-hex-1-yloxy)benzoic acid (0.47 g, 0.0016 mol) in THF (7.29 g) was added dropwise to the mixture and stirred at 0° C. for 2 hours. After a solution of TEA (0.19 g, 0.00192 mol) and DMAP (0.002 g) in THF (7.29 g) was further added to the mixture, 9,10-bis(4-hydroxyphenyl)anthracene (0.29 g, 0.0008 mol) obtained in step 1 was added to the mixture. The mixture was stirred at room temperature overnight. The organic layer was extracted. After the solvent was removed by distillation, the residue was separated by silica gel column chromatography (eluent: chloroform). The separated product was crystallized from chloroform/methanol and dried under reduced pressure at 40° C. to give 0.41 g of a white solid (56.3percent yield).
 

Historical Records

Technical Information

Categories