1352733-99-3 Usage
Description
(2-Fluoro-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)Methanol, also known as TFBM, is a chemical compound characterized by its fluorinated alcohol structure and a boron-containing aromatic ring. It serves as a reagent in chemical reactions and organic synthesis, playing a crucial role in the synthesis of various organic molecules. TFBM is a versatile and important building block in the development of pharmaceuticals, agrochemicals, and materials science, valued for its unique structure and properties, making it an essential tool for researchers and chemists in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
TFBM is used as a key intermediate in the synthesis of pharmaceutical compounds for [application reason]. Its unique structure allows for the development of new drugs with improved properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Agrochemical Industry:
TFBM is used as a building block in the creation of agrochemicals for [application reason]. Its incorporation into agrochemical formulations can lead to the development of more effective and environmentally friendly pesticides, herbicides, and other agricultural products.
Used in Materials Science:
TFBM is used as a component in the development of advanced materials for [application reason]. Its unique properties can contribute to the creation of materials with improved performance characteristics, such as enhanced mechanical strength, thermal stability, or electrical conductivity.
Used in Organic Chemistry Research:
TFBM is used as a reagent and building block in organic chemistry research for [application reason]. Its versatility and unique structure make it an invaluable tool for chemists exploring new reaction pathways, developing novel synthetic methods, and discovering new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1352733-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,7,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352733-99:
(9*1)+(8*3)+(7*5)+(6*2)+(5*7)+(4*3)+(3*3)+(2*9)+(1*9)=163
163 % 10 = 3
So 1352733-99-3 is a valid CAS Registry Number.
1352733-99-3Relevant articles and documents
Para-Selective, Iridium-Catalyzed C-H Borylations of Sulfated Phenols, Benzyl Alcohols, and Anilines Directed by Ion-Pair Electrostatic Interactions
Montero Bastidas, Jose R.,Oleskey, Thomas J.,Miller, Susanne L.,Smith, Milton R.,Maleczka, Robert E.
, p. 15483 - 15487 (2019/10/11)
Para C-H borylations (CHB) of tetraalkylammonium sulfates and sulfamates have been achieved using bipyridine-ligated Ir boryl catalysts. Selectivities can be modulated by both the length of the alkyl groups in the tetraalkylammonium cations and the substituents on the bipyridine ligands. Ion pairing, where the alkyl groups of the cation shield the meta C-H bonds in the counteranions, is proposed to account for para selectivity. The 4,4′-dimethoxy-2,2′-bipyridine ligand gave superior selectivities.
NRF2 REGULATORS
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Page/Page column 177; 180; 182; 185;, (2015/07/07)
The present invention relates to bis aryl analogs, pharmaceutical compositions containing them and their use as Nrf2 regulators.
ANTIDIABETIC TRICYCLIC COMPOUNDS
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Page/Page column 76, (2014/02/16)
Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.
