1384216-47-0 Usage
Uses
Used in Pharmaceutical Industry:
[5-chloro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyldimethylamine serves as a reagent in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for specific chemical reactions that are crucial in the creation of medicinally relevant molecules.
Used in Agrochemical Industry:
In the agrochemical sector, {[5-chloro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}dimethylamine is utilized for the synthesis of agrochemicals, including pesticides and herbicides. Its role in these applications is to facilitate the production of compounds that can effectively control, repel, or kill pests, thereby protecting crops and enhancing agricultural productivity.
Used in Research and Development:
[5-chloro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyldimethylamine is employed in the research and development of new chemical compounds, where it may be used to explore novel reactions, synthesize potential lead compounds, or study the properties of new materials.
Used in Production of Fine Chemicals:
[5-chloro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyldimethylamine is also used in the production of fine chemicals, which are high-purity chemicals often used in various specialized applications, such as in the fragrance, flavor, or chemical intermediate industries. Its presence in these processes ensures the synthesis of high-quality end products with specific characteristics required by these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1384216-47-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,2,1 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384216-47:
(9*1)+(8*3)+(7*8)+(6*4)+(5*2)+(4*1)+(3*6)+(2*4)+(1*7)=160
160 % 10 = 0
So 1384216-47-0 is a valid CAS Registry Number.
1384216-47-0Relevant articles and documents
Role of hemilabile diamine ligands in the amine-directed C-H borylation of arenes
Hale, Lillian V. A.,McGarry, Kathryn A.,Ringgold, Marissa A.,Clark, Timothy B.
supporting information, p. 51 - 55 (2015/01/30)
A study of the role played by the bidentate ligand used in amine-directed C-H borylation is described. Both reaction conversion and selectivity were significantly impacted when steric congestion and electronic perturbations of the bidentate diamine ligand were made, but a more significant influence was imparted by reducing the bite angle of the ligand. N-Benzylaminopyridine was identified as a general ligand that improves both selectivity and yield for most problematic substrates previously reported with picolylamine as ligand.
Iridium-catalyzed, substrate-directed C-H borylation reactions of benzylic amines
Roering, Andrew J.,Hale, Lillian V. A.,Squier, Phillip A.,Ringgold, Marissa A.,Wiederspan, Emily R.,Clark, Timothy B.
, p. 3558 - 3561 (2012/08/29)
The iridium-catalyzed arene C-H borylation reaction of benzylic amines has been developed, which inverts the typical steric-controlled product distribution to provide ortho-substituted boronate esters. Picolylamine was found to be an ideal ligand to replace 4,4′-di-tert-butylbipyridine to induce the directing effect. Preliminary experiments are consistent with a mechanism involving dissociation of one amine of the hemilabile diamine ligand.
