1544673-40-6 Usage
Uses
Used in Organic Synthesis:
(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is used as a reagent in organic synthesis for the production of other chemicals. Its unique structure and functional groups make it a valuable component in creating a variety of compounds.
Used in Suzuki Coupling Reactions:
In the field of organic chemistry, (4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is used as a building block for Suzuki coupling reactions, which are a common method for forming carbon-carbon bonds. Its boron-containing ring plays a crucial role in this process.
Used in Pharmaceutical Development:
(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is used as a key intermediate in the development of various pharmaceuticals. Its versatility and reactivity in chemical reactions contribute to the synthesis of potential drug candidates.
Used in Agrochemical Production:
(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is also utilized in the production of agrochemicals, where its properties can be harnessed to create effective and targeted products for agricultural applications.
Used in Specialty Chemicals:
(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is used as a component in the creation of specialty chemicals, where its unique attributes can be applied to develop specific industrial or commercial products.
Check Digit Verification of cas no
The CAS Registry Mumber 1544673-40-6 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, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1544673-40:
(9*1)+(8*5)+(7*4)+(6*4)+(5*6)+(4*7)+(3*3)+(2*4)+(1*0)=176
176 % 10 = 6
So 1544673-40-6 is a valid CAS Registry Number.
1544673-40-6Relevant 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.
