1329422-57-2 Usage
Uses
Used in Chemical Synthesis:
N-methyliminodiacetyl (1-(4-fluorophenyl)-2-oxoethyl)boronate is used as a synthetic intermediate for the preparation of various organic compounds. Its α-MIDA boryl aldehyde structure allows for versatile synthetic transformations, making it a valuable building block in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the pharmaceutical industry, N-methyliminodiacetyl (1-(4-fluorophenyl)-2-oxoethyl)boronate is used as a key component in the development of novel drug candidates. Its unique structure can be exploited to design and synthesize new bioactive molecules with potential therapeutic applications.
Used in Catalyst Design:
N-methyliminodiacetyl (1-(4-fluorophenyl)-2-oxoethyl)boronate is also used as a catalyst or catalyst precursor in various chemical reactions. Its boryl aldehyde functionality can be employed to facilitate selective transformations, enhancing the efficiency and selectivity of catalytic processes.
Used in Material Science:
In the field of materials science, N-methyliminodiacetyl (1-(4-fluorophenyl)-2-oxoethyl)boronate can be utilized in the development of new materials with unique properties. Its incorporation into polymers or other materials can lead to the creation of materials with improved performance characteristics, such as enhanced stability or specific binding properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1329422-57-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,9,4,2 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1329422-57:
(9*1)+(8*3)+(7*2)+(6*9)+(5*4)+(4*2)+(3*2)+(2*5)+(1*7)=152
152 % 10 = 2
So 1329422-57-2 is a valid CAS Registry Number.
1329422-57-2Relevant academic research and scientific papers
Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates
St. Denis, Jeffrey D.,Lee, C. Frank,Yudin, Andrei K.
supporting information, p. 5764 - 5767 (2015/12/11)
Herein, we describe the rhodium-catalyzed C-H amination reaction of 1,2-boryl sulfamate esters derived from amphoteric α-boryl aldehydes. Depending on the substitution pattern of the boryl sulfamate ester, a diverse range of five- or six-membered ring heterocycles are accessible using this transformation. The highly chemoselective nature of the C-H functionalization reaction preserves the alkyl boronate functional group, which enables the synthesis of B-C-N and B-C-C-N motifs that are present in a number of hydrolase inhibitors.
Amphoteric α-boryl aldehydes
He, Zhi,Yudin, Andrei K.
, p. 13770 - 13773 (2011/10/05)
A new class of stable molecules, α-boryl aldehydes, has been prepared from oxiranyl N-methyliminodiacetyl boronates by a 1,2-boryl migration with concomitant epoxide scission. A range of boryl imines, alkenes, alcohols, acids, enol ethers, enamides, and other functionalized boronic acid derivatives that are difficult or impossible to prepare using established protocols can be accessed from α-boryl aldehydes. The chemoselective transformations of these building blocks, including the facile synthesis of functionalized unnatural amino acids from silyloxy and amido vinyl boronates, attest to the potential of α-boryl aldehydes in chemical synthesis.
