328956-60-1 Usage
Uses
Used in Pharmaceutical Industry:
3-Fluoro-5-formylphenylboronic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to participate in cross-coupling reactions allows for the formation of complex organic molecules with potential therapeutic properties. It is particularly valuable in the development of new drugs and the modification of existing ones to improve their efficacy and safety.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Fluoro-5-formylphenylboronic acid is utilized as a reagent in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure and reactivity enable the creation of novel compounds with improved performance and selectivity, contributing to more effective and environmentally friendly agricultural practices.
Used in Materials Science:
3-Fluoro-5-formylphenylboronic acid is employed as a building block in the development of advanced materials with specific properties. Its incorporation into polymers, coatings, and other materials can enhance their performance, durability, and functionality. This makes it a valuable component in the design and synthesis of materials for various applications, including electronics, automotive, and aerospace industries.
Used in Organometallic Chemistry:
3-Fluoro-5-formylphenylboronic acid is used as a ligand in organometallic chemistry, where it plays a crucial role in the stabilization and reactivity of metal complexes. Its presence can influence the electronic properties and catalytic activity of these complexes, making it an important component in the development of new catalysts and organometallic compounds for various applications, such as in chemical synthesis and catalysis.
Used in Chemical Research:
As a versatile reagent, 3-Fluoro-5-formylphenylboronic acid is extensively used in chemical research to explore new reaction pathways, develop novel synthetic methods, and investigate the fundamental properties of boronic acid derivatives. Its unique structure and reactivity make it an ideal candidate for studying the mechanisms of cross-coupling reactions and other organic transformations, contributing to the advancement of organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 328956-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,9,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 328956-60:
(8*3)+(7*2)+(6*8)+(5*9)+(4*5)+(3*6)+(2*6)+(1*0)=181
181 % 10 = 1
So 328956-60-1 is a valid CAS Registry Number.
