221006-71-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromo-2-methylphenylboronic acid is used as a Toll-like receptor (TLR) inhibitor for the treatment of inflammatory and autoimmune diseases. Its ability to modulate immune responses makes it a promising candidate for therapeutic intervention in conditions such as rheumatoid arthritis, lupus, and inflammatory bowel disease.
In addition to its role as a TLR inhibitor, 4-Bromo-2-methylphenylboronic acid may also find applications in other areas of pharmaceutical research, such as the development of new drugs targeting specific receptors or enzymes, or as a building block for the synthesis of more complex organic molecules with potential therapeutic properties.
Used in Materials Science:
4-Bromo-2-methylphenylboronic acid can be utilized in the development of new materials with unique properties, such as organic semiconductors, sensors, or catalysts. Its structural features, including the boron atom and the bromine and methyl substituents, may contribute to the formation of novel materials with enhanced performance in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 221006-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,0,0 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 221006-71:
(8*2)+(7*2)+(6*1)+(5*0)+(4*0)+(3*6)+(2*7)+(1*1)=69
69 % 10 = 9
So 221006-71-9 is a valid CAS Registry Number.
221006-71-9Relevant academic research and scientific papers
Side functionalization of diboronic acid precursors for covalent organic frameworks
Faury, Thomas,Dumur, Frederic,Clair, Sylvain,Abel, Mathieu,Porte, Louis,Gigmes, Didier
, p. 2067 - 2075 (2013/04/23)
A series of substituted 1,4-benzenediboronic acids (BDBA) was synthesized and their thermal properties investigated. Two diboronic acids were studied as building-blocks for covalent organic framework (COF) formation, namely 2,5-dimethoxy-1,4-benzenediboronic acid and 2-nitro-1,4-benzeneboronic acid. Interestingly, substitution of the BDBA core caused a dramatic decrease of the polymerization temperature leading to the formation of a less organized structure.
