Home Cart Sign in  
Chemical Structure| 50487-72-4 Chemical Structure| 50487-72-4
Chemical Structure| 50487-72-4

*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

Product Citations

Barteczko, Natalia ; Grymel, Miroslawa ; Erfurt, Karol ; Jakobik-Kolon, Agata ; Brzeczek-Szafran, Alina ; Chrobok, Anna

Abstract: Ring-closing metathesis of a model substrate, di-Et diallylmalonate, was used to study a new catalytic system based on the com. available HG2 catalyst and ionic liquids derived from -glucose employed as surfactants in an aqueous metathesis reaction. The quantity, structure, and concentration of -glucose-based bromides were optimized to obtain high product yield and purity. (N-[2-(β--glucopyranosyloxy)ethyl]-N,N-dimethyl-N-dodecyl-ammonium bromide) was the most active surfactant, with a critical micelle concentration of 0.020 mol/dm3. HG2 was used in truly catalytic amounts (0.2 mol%) at 25 °C, enabling the synthesis of product in 180 min. High conversion (88%) and selectivity (100%), with low Ru content in the product, were obtained. Five cycles of a model metathesis reaction could be conducted without the loss of surfactant activity and with low Ru content in the product. 1H NMR spectroscopic studies showed the formation of micelles and the transformation of the substrate, in the presence of the catalyst, to product.

Keywords: Ring-closing metathesis ; D-glucose-based ionic liquids ; Micellar catalysis ; Ru content ; Carbohydrate ; Bio -based surfactants

Purchased from AmBeed:

Alternative Products

Product Details of N,N-Diallyl-4-methylbenzenesulfonamide

CAS No. :50487-72-4
Formula : C13H17NO2S
M.W : 251.35
SMILES Code : O=S(C1=CC=C(C)C=C1)(N(CC=C)CC=C)=O
MDL No. :MFCD00226469
InChI Key :OKXHMBXWZHCSMR-UHFFFAOYSA-N
Pubchem ID :351447

Safety of N,N-Diallyl-4-methylbenzenesulfonamide

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338
 

Historical Records

Technical Information

Categories