480424-69-9 Usage
Uses
Used in Pharmaceutical Synthesis:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex molecular structures. Its reactivity and stability under various conditions make it a preferred choice for developing new drugs with improved efficacy and safety profiles.
Used in Agrochemical Development:
In the agrochemical industry, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate serves as a crucial building block for the synthesis of novel agrochemicals. Its application aids in the development of more effective and environmentally friendly pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Used in Material Science:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is employed as a versatile component in the synthesis of advanced materials. Its unique properties contribute to the creation of materials with specific characteristics, such as improved mechanical strength, thermal stability, or electrical conductivity, which are essential for various industrial applications.
Used in Organic Chemistry Research:
As a reagent in organic chemistry, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is used to explore new reaction pathways and mechanisms. Its compatibility with a wide range of conditions allows researchers to investigate its potential in various chemical transformations, leading to the discovery of innovative synthetic methods and the development of new compounds with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 480424-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,0,4,2 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 480424-69:
(8*4)+(7*8)+(6*0)+(5*4)+(4*2)+(3*4)+(2*6)+(1*9)=149
149 % 10 = 9
So 480424-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H19BO4/c1-10(16)17-12-8-6-7-11(9-12)15-18-13(2,3)14(4,5)19-15/h6-9H,1-5H3
480424-69-9Relevant academic research and scientific papers
Directed ortho borylation of phenol derivatives catalyzed by a silica-supported iridium complex
Yamazaki, Kenji,Kawamorita, Soichiro,Ohmiya, Hirohisa,Sawamura, Masaya
supporting information; experimental part, p. 3978 - 3981 (2010/10/21)
The directed ortho borylation of phenol derivatives protected with an N,N-diethylcarbamoyl group was efficiently catalyzed by an immobilized monophosphine-Ir system, which was prepared in situ from [Ir(OMe)(cod)] 2 and a silica-supported, compact phosphine. The utility of the carbamoyloxy group as a leaving group for metal-catalyzed cross-coupling reactions was demonstrated by its utilization in the synthesis of a terphenyl derivative.
