1544673-68-8 Usage
Uses
Used in Pharmaceutical Industry:
[4-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is used as a building block for the development of new pharmaceuticals due to its ability to form carbon-carbon and carbon-heteroatom bonds, which are essential in the creation of various drug molecules.
Used in Agrochemical Industry:
In the agrochemical industry, [4-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is used as a key component in the synthesis of new agrochemicals, contributing to the development of innovative products for agricultural applications.
Used in Material Science:
[4-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is utilized as a versatile reagent in material science for the formation of novel materials with specific properties, such as improved strength, durability, or chemical resistance.
Used in Chemical Research:
This organoboron compound is also used as a valuable tool in chemical research, where its unique reactivity and structure enable the exploration of new chemical reactions and the synthesis of complex molecules for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1544673-68-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,4,6,7 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1544673-68:
(9*1)+(8*5)+(7*4)+(6*4)+(5*6)+(4*7)+(3*3)+(2*6)+(1*8)=188
188 % 10 = 8
So 1544673-68-8 is a valid CAS Registry Number.
1544673-68-8Relevant academic research and scientific papers
Synthesis of boron-containing primary amines
Chung, Sheng-Hsuan,Lin, Ting-Ju,Hu, Qian-Yu,Tsai, Chia-Hua,Pan, Po-Shen
, p. 12346 - 12367 (2013/11/06)
In this study, boron-containing primary amines were synthesized for use as building blocks in the study of peptoids. In the first step, Gabriel synthesis conditions were modified to enable the construction of seven different aminomethylphenyl boronate esters in good to excellent yields. These compounds were further utilized to build peptoid analogs via an Ugi four-component reaction (Ugi-4CR) under microwave irradiation. The prepared Ugi-4CR boronate esters were then successfully converted to the corresponding boronic acids. Finally, the peptoid structures were successfully modified by cross-coupling to aryl/heteroaryl chlorides via a palladium-mediated Suzuki coupling reaction to yield the corresponding derivatives in moderate to good yields.
