627906-52-9

Usage

Uses

Used in Organic Synthesis:
TMPD-Borane is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial in the creation of complex organic molecules and pharmaceuticals.
Used in Polymer Industry:
In the polymer industry, TMPD-Borane is utilized as a stabilizer in radical polymerization reactions, contributing to the control of polymer structure and properties.
Used in Preparation of Boron Compounds:
TMPD-Borane serves as a boron source in the preparation of a variety of boron compounds, which have applications in different fields such as pharmaceuticals, materials science, and chemical research.
Used in Antioxidant Applications for Polymers:
It has been investigated for its potential use as an antioxidant in polymers, which could enhance the stability and longevity of polymer-based materials.
Used in Lithium-Ion Batteries:
TMPD-Borane has been considered for use as a stabilizer in lithium-ion batteries, potentially improving their performance and safety.
Used in Chemical Research:
Due to its reactivity and unique properties, TMPD-Borane is also used in chemical research to explore new reaction pathways and develop novel synthetic methods.

Upstream product

• 2362-12-1 4-Bromo-2-methylphenol 
• 73183-34-3 bis(pinacol)diborane 
• 95-48-7 ortho-cresol 

Downstream Products

• 627906-53-0 2-{4-[2-(11-ethyl-6,11-dihydro-5-methyl-6-oxo-5H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-8-yl)ethoxy]-3-methylphenyl}-4,4,5,5-tetramethyl-1,3,2-dioxoborolane 
• 2165340-32-7 HY-112667 
• 762263-66-1 (4-hydroxy-3-methylphenyl)boronic acid 

Relevant academic research and scientific papers

TOLL-LIKE RECEPTOR 8 (TLR8)-SPECIFIC ANTAGONISTS AND METHODS OF MAKING AND USES THEREOF

Toll-like receptor 8 (TLR8)-specific inhibitors and methods of using the same in individuals having an autoimmune disease or an inflammatory disorder.

Para-Selective, Iridium-Catalyzed C-H Borylations of Sulfated Phenols, Benzyl Alcohols, and Anilines Directed by Ion-Pair Electrostatic Interactions

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.

BIARYL DERIVATIVES AS GPR120 AGONISTS

The present invention relates to biaryl derivatives of Formula 1, a method for preparing the same, a pharmaceutical composition comprising the same and use thereof. The biaryl derivatives of Formula 1 according to the present invention promote GLP-1 formation in the gastrointestinal tract and improve insulin resistance in the liver or in muscle due to anti-inflammatory action in macrophages, lipocytes, etc., and can accordingly be effectively used for preventing or treating diabetes, complications of diabetes, obesity, non-alcoholic fatty liver, steatohepatitis, osteoporosis or inflammation.

Synthesis of substituted asymmetrical biphenyl amino esters as alpha helix mimetics

As part of our ongoing project to develop new molecular probes for estrogen receptor-alpha, we are exploring the utility of internally-substituted asymmetric biphenyls as a proteomimetic scaffold. In this study, we describe synthetic methods for preparing

Non-nucleoside reverse transcriptase inhibitors

Compounds represented by formula I: wherein R2 is selected from the group consisting of H, (C1-4)alkyl, halo, haloalkyl, OH, (C1-6)alkoxy, NH(C1-4alkyl) or N(C1-4alkyl)2; R4 is H