1426804-80-9 Usage
Description
2-(2-Chloro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic acid derivative with a chloro-nitrophenyl group attached to the boron atom. It is a chemical compound used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, a widely used method for forming carbon-carbon bonds. 2-(2-Chloro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is highly valuable in the field of medicinal chemistry and material science for the synthesis of complex molecular structures. It is also known for its stability and compatibility with a wide range of reaction conditions, making it a versatile tool for chemical synthesis.
Uses
Used in Organic Synthesis:
2-(2-Chloro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is a widely used method for forming carbon-carbon bonds. It is particularly valuable in the field of medicinal chemistry and material science for the synthesis of complex molecular structures.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-(2-Chloro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a key intermediate in the synthesis of various drug molecules. Its stability and compatibility with a wide range of reaction conditions make it a versatile tool for the development of new pharmaceutical compounds.
Used in Material Science:
In the field of material science, 2-(2-Chloro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used for the synthesis of advanced materials with specific properties. Its versatility in chemical synthesis allows for the creation of complex molecular structures that can be utilized in various applications, such as in the development of new materials with unique electronic, optical, or mechanical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1426804-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,8,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1426804-80:
(9*1)+(8*4)+(7*2)+(6*6)+(5*8)+(4*0)+(3*4)+(2*8)+(1*0)=159
159 % 10 = 9
So 1426804-80-9 is a valid CAS Registry Number.
1426804-80-9Relevant articles and documents
Synthesis of trimethylstannyl arylboronate compounds by sandmeyer-type transformations and their applications in chemoselective cross-coupling reactions
Qiu, Di,Wang, Shuai,Tang, Shengbo,Meng, He,Jin, Liang,Mo, Fanyang,Zhang, Yan,Wang, Jianbo
, p. 1979 - 1988 (2014/04/03)
A synthetic method based on Sandmeyer-type reactions to access both tin- and boron-substituted arenes from nitroaniline derivatives is described. This transformation can be applied to the synthesis of a series of functionalized trimethylstannyl arylboronates. In addition, the chemoselective reaction of the Stille and Suzuki-Miyaura cross-coupling reactions is explored, and a series of m- and p-terphenyl derivatives have been synthesized by conducting consecutive one-pot Stille and Suzuki-Miyaura cross-coupling reactions.
