1618099-49-2 Usage
Uses
Used in Organic Synthesis:
(E)-2-(3,4-dimethoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent for cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Its unique reactivity and properties make it a valuable tool in organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-2-(3,4-dimethoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used for the synthesis of various biologically active compounds. Its versatility in chemical reactions allows for the creation of a wide range of pharmaceutical products.
Used in Material Science:
(E)-2-(3,4-dimethoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane has potential applications in material science, particularly in the synthesis of functionalized polymers and organic electronic materials. Its unique properties contribute to the development of advanced materials with specific functionalities.
Overall, (E)-2-(3,4-dimethoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane plays a crucial role in various chemical processes and has diverse applications in different fields, including organic synthesis, pharmaceuticals, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 1618099-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,8,0,9 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1618099-49:
(9*1)+(8*6)+(7*1)+(6*8)+(5*0)+(4*9)+(3*9)+(2*4)+(1*9)=192
192 % 10 = 2
So 1618099-49-2 is a valid CAS Registry Number.
1618099-49-2Relevant academic research and scientific papers
Stereoselective synthesis of trisubstituted alkenes via cobalt-catalyzed double dehydrogenative borylations of 1-alkenes
Wen, Huanan,Zhang, Lei,Zhu, Suzhen,Liu, Guixia,Huang, Zheng
, p. 6419 - 6425 (2017/11/09)
A highly selective cobalt-catalyzed single and double dehydrogenative borylations (DHBs) of terminal alkenes have been developed for the synthesis of trans-monoborylalkenes and diborylalkenes, respectively. While the cobalt-catalyzed double DHBs of aryl 1
Ruthenium-catalyzed one-pot synthesis of (E)-(2-arylvinyl)boronates through an isomerization/cross-metathesis sequence from allyl-substituted aromatics
Hemelaere, Remy,Caijo, Frederic,Mauduit, Marc,Carreaux, Francois,Carboni, Bertrand
supporting information, p. 3328 - 3333 (2014/06/09)
We described the efficient preparation of (E)-(2-arylvinyl)boronates from allylbenzene derivatives on the basis of an isomerization/cross-metathesis sequence catalyzed by a modified Hoveyda-Grubbs catalyst. The implementation of the experimental procedure was simple and compatible with a large variety of substrates. This methodology provides a new chemical transformation not described to date. Allyl-substituted aromatics can thus be converted into diversely functionalized compounds, such as (E)-stilbene derivatives or (E)-vinyl azides, in only two steps. Copyright
