159119-10-5 Usage
Description
2-Fluoro-4-(trans-propylcyclohexyl)phenyl boronic acid is a boronic acid derivative with the molecular formula C15H21BFO2. It features a fluoro and cyclohexyl group, along with a trans-propyl chain attached to a phenyl ring. This chemical compound is known for its role in organic synthesis, particularly as a building block for the creation of pharmaceuticals, agrochemicals, and materials with potential therapeutic or industrial applications.
Uses
Used in Pharmaceutical Industry:
2-Fluoro-4-(trans-propylcyclohexyl)phenyl boronic acid is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its ability to form carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions makes it a valuable tool in medicinal chemistry, enabling the creation of diverse and complex molecular structures with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Fluoro-4-(trans-propylcyclohexyl)phenyl boronic acid serves as a key component in the synthesis of novel agrochemicals. Its reactivity in cross-coupling reactions allows for the design and synthesis of new pesticides, herbicides, and other agrochemicals with improved efficacy and selectivity, contributing to more sustainable agricultural practices.
Used in Materials Science:
2-Fluoro-4-(trans-propylcyclohexyl)phenyl boronic acid is utilized as a building block in the development of advanced materials for various applications within materials science. Its unique structural features and reactivity in cross-coupling reactions facilitate the synthesis of new polymers, coatings, and other materials with tailored properties, such as improved mechanical strength, thermal stability, or specific interactions with biological systems.
Overall, 2-Fluoro-4-(trans-propylcyclohexyl)phenyl boronic acid is a versatile chemical compound with significant applications across multiple industries, including pharmaceuticals, agrochemicals, and materials science. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it an essential component in the synthesis of innovative compounds with potential applications in healthcare, agriculture, and various other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 159119-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159119-10:
(8*1)+(7*5)+(6*9)+(5*1)+(4*1)+(3*9)+(2*1)+(1*0)=135
135 % 10 = 5
So 159119-10-5 is a valid CAS Registry Number.
159119-10-5Relevant articles and documents
Liquid crystal compound containing dimethylbenzene and difluoromethylenedioxy linking group and application thereof
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, (2021/09/01)
The invention discloses a liquid crystal compound containing a dimethylbenzene and difluoromethyleneoxy linking group and application of the liquid crystal compound. The compound is as shown in formula I. In the molecular structure of the compound as show
