876169-22-1 Usage
Description
(E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is a boronic ester chemical compound with the molecular formula C16H21BO4. It is widely utilized in organic synthesis and serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials. (E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is distinguished by the presence of a boron atom in its structure, which endows it with unique reactivity and properties. It is also recognized for its application in Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds in organic chemistry. Furthermore, it has garnered interest for its potential use in the development of innovative materials and drug discovery processes.
Uses
Used in Pharmaceutical Industry:
(E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is used as a synthetic intermediate for the development of new pharmaceuticals. Its unique boron-containing structure allows for the creation of a diverse range of biologically active molecules, contributing to the advancement of drug discovery.
Used in Agrochemical Industry:
In the agrochemical industry, (E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is employed as a building block for the synthesis of novel agrochemicals. Its reactivity and properties enable the development of innovative compounds with potential applications in pest control, crop protection, and other agricultural areas.
Used in Material Science:
(E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is used as a key component in the development of new materials. Its unique properties and reactivity make it a valuable asset in the creation of advanced materials with potential applications in various industries, such as electronics, automotive, and aerospace.
Used in Organic Chemistry:
(E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is utilized as a valuable tool in organic chemistry, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. (E)-ethyl 3-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate's boron atom enhances the efficiency and selectivity of these reactions, making it an indispensable tool for chemists working in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 876169-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,1,6 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 876169-22:
(8*8)+(7*7)+(6*6)+(5*1)+(4*6)+(3*9)+(2*2)+(1*2)=211
211 % 10 = 1
So 876169-22-1 is a valid CAS Registry Number.
876169-22-1Relevant articles and documents
NOVEL COMPOUNDS THAT MODULATE PPARγ TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS
-
Page/Page column 35, (2010/11/08)
The invention relates to novel compounds corresponding to the general formula (I) below: and also to the method for preparing them, and to their use in pharmaceutical compositions intended for use in human or veterinary medicine (in dermatology, and also
