Home Cart Sign in  
Chemical Structure| 4026-05-5 Chemical Structure| 4026-05-5

Structure of 4026-05-5

Chemical Structure| 4026-05-5

*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 [ 4026-05-5 ]

CAS No. :4026-05-5
Formula : C10H14O2
M.W : 166.22
SMILES Code : CC(C)(C)C1=CC=CC(O)=C1O
MDL No. :MFCD00515124

Safety of [ 4026-05-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 4026-05-5 ]

* 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 [ 4026-05-5 ]

[ 4026-05-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4026-05-5 ]
  • [ 38573-88-5 ]
  • C23H23NO2 [ No CAS ]
  • C23H23NO2 [ No CAS ]
  • 2
  • [ 4026-05-5 ]
  • [ 38573-88-5 ]
  • C16H15BrO2 [ No CAS ]
  • C16H15BrO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.8 g; 1.4 g With caesium carbonate; In 1-methyl-pyrrolidin-2-one; at 190℃; for 4h; In a 0.5 L reaction flask, 3.0 g (18.0 mmol) of 3-tert-butylbenzene-1,2-diol,7.0 g (36.1 mmol) of <strong>[38573-88-5]1-<strong>[38573-88-5]bromo-2,3-difluorobenzene</strong></strong>,11.8 g (36.1 mmol) of cesium carbonate,myriad N-methylpyrrolidone. And the mixture was stirred at 190 for 4 hours.After the completion of the reaction, the temperature was lowered, toluene and distilled water were added to separate layers, and the obtained organic layer was distilled under reduced pressure. This mixture was purified by column chromatography to prepare 0.8 g (14 wtpercent) of intermediate compound [A-1] and 1.4 g (25 wtpercent) of [A-2].
 

Historical Records

Technical Information

Categories