Home Cart Sign in  
Chemical Structure| 562098-08-2 Chemical Structure| 562098-08-2

Structure of 562098-08-2

Chemical Structure| 562098-08-2

*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 [ 562098-08-2 ]

CAS No. :562098-08-2
Formula : C15H21BO4
M.W : 276.14
SMILES Code : O=C(OCC2(=CC=C(B1(OC(C)(C)C(O1)(C)C))C=C2))C
MDL No. :MFCD02179494

Safety of [ 562098-08-2 ]

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

Application In Synthesis of [ 562098-08-2 ]

* 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 [ 562098-08-2 ]

[ 562098-08-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-36-5 ]
  • [ 302348-51-2 ]
  • [ 562098-08-2 ]
YieldReaction ConditionsOperation in experiment
With dmap; triethylamine; In tetrahydrofuran; at 20℃; for 1h; [4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol (500 mg) and DMAP (26 mg) were dissolved in THF (7.1 mL), followed by the addition of TEA (0.74 mL). At room temperature, acetylchloride (0.23 mL) was addedthereto, followed by stirring for 1 hour. Ethyl acetate was added thereto, and the resulting mixture was washed sequentiallywith water and saturated brine. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilledoff. The residue was purified by silica gel column chromatography (mobile phase: hexane/ethyl acetate) to give [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl acetate.
 

Historical Records

Categories