1544673-71-3 Usage
Uses
Used in Pharmaceutical Development:
[4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is used as a reagent in the pharmaceutical industry for the development of new drugs. Its unique reactivity and molecular structure allow for the creation of novel compounds with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, [4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is used as a reagent for the synthesis of new agrochemicals. Its distinctive properties can contribute to the development of innovative products with improved performance and efficiency in agriculture.
Used in Material Science:
[4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine is also utilized in material science as a reagent for the development of new materials. [4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine's unique properties can be harnessed to create materials with enhanced characteristics, such as improved strength, durability, or chemical resistance.
It is crucial to handle and use [4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine with caution, as boron-containing compounds can be toxic and pose health risks if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 1544673-71-3 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, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1544673-71:
(9*1)+(8*5)+(7*4)+(6*4)+(5*6)+(4*7)+(3*3)+(2*7)+(1*1)=183
183 % 10 = 3
So 1544673-71-3 is a valid CAS Registry Number.
1544673-71-3Relevant 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.
