355836-08-7

Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dimethyl-6-methoxyphenylboronic Acid is used as a building block in medicinal chemistry for the synthesis of complex molecules. It is particularly valuable in drug discovery and chemical biology, where its unique structure contributes to the development of new therapeutic agents.
Used in Scientific Research:
In the field of scientific research, 2,4-Dimethyl-6-methoxyphenylboronic Acid is used as a reagent in various chemical reactions, such as the Suzuki coupling process. This process is essential for creating more complex molecules that can be further studied or utilized in the development of new compounds and materials.
Used in Chemical Biology:
2,4-Dimethyl-6-methoxyphenylboronic Acid is employed as a key component in the construction of biologically active molecules. Its presence in these molecules can help in understanding the interactions between small molecules and biological targets, which is crucial for the advancement of chemical biology research.

InChI:InChI=1/C9H13BO3/c1-6-4-7(2)9(10(11)12)8(5-6)13-3/h4-5,11-12H,1-3H3

Upstream product

• 874-63-5 3,5-dimethylmethoxybenzene 
• 121-43-7 Trimethyl borate 

Downstream Products

• 360576-58-5 3-methoxy-2-(4-methoxy-6-methyl-5-nitropyrimidin-2-yl)-1,5-dimethylbenzene 
• 1067229-14-4 C₂₀H₂₈N₂O₃ 
• 1067228-88-9 C₂₀H₂₉N₃O 
• 1411858-67-7 2’-methoxy-4’,6’-dimethylisoflavanone 
• 475171-70-1 N-(cyclopropylmethyl)-2-ethyl-7-(2-methoxy-4,6-dimethylphenyl)-N-[(tetrahydrofuran-3-yl)methyl]pyrazolo[1,5-a]pyridin-3-amine 
• 475171-69-8 N-(cyclopropylmethyl)-2-ethyl-7-(2-methoxy-4,6-dimethylphenyl)-N-[(tetrahydrofuran-2-yl)methyl]pyrazolo[1,5-a]pyridin-3-amine 
• 475171-68-7 N-(cyclopropylmethyl)-2-ethyl-N-(3-fluoropropyl)-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-amine 
• 1380434-44-5 tert-butyl [2-ethyl-7-(2-methoxy-4,6-dimethylphenyl)-pyrazolo[1,5-a]pyridin-3-yl]carbamate 
• 475171-67-6 N-(cyclopropylmethyl)-2-ethyl-7-(2-methoxy-4,6-dimethylphenyl)-N-(2-methoxyethyl)pyrazolo[1,5-a]pyridin-3-amine 
• 475171-41-6 N,N-bis(cyclopropylmethyl)-2-ethyl-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-amine 
• 478036-12-3 4-methoxy-2-(6-methoxy-2,4-dimethylphenyl)-6-methylpyrimidin-5-ol 
• 355836-13-4 C₁₅H₁₈N₂O 

Relevant academic research and scientific papers

NLRP3 INFLAMMASOME INHIBITORS

The present invention relates to novel pyridazin-3-yl phenol compounds of Formula (I): wherein R1, R2, R3, R4, R5 and Z are defined herein, which inhibit NOD-like receptor protein 3 (NLRP3) inflammaso

A transition metal complex compound, and the compound of the catalyst and a catalyst for large amt. pentavelent carried out in the presence of an olefin multimer manufacturing method

PROBLEM TO BE SOLVED: To provide a transition metal complex compound, to provide an olefin polymerizing catalyst, containing the compound, and having excellent activity, and to provide a method for producing the olefin polymer which is carried out in the presence of the catalyst.SOLUTION: There is provided the transition metal complex compound of compound 3, e.g. of chemical formula; and the olefin polymerizing catalyst including following components (A) and (B): (A) the transition metal compound; and (B) at least one compound selected from the group consisting of (B-1) an organometallic compound, (B-2) an organoaluminumoxy compound, and (B-3) a compound reactive with the transition metal compound (A), and forming an ion pair.

2-Arylpyrimidines: Novel CRF-1 receptor antagonists

The design, synthesis and structure-activity relationship studies of a novel series of CRF-1 receptor antagonists, the 2-arylpyrimidines, are described. The effects of substitution on the aromatic ring and the pyrimidine core on CRF-1 receptor binding wer