590401-47-1 Usage
Uses
Used in Organic Synthesis:
Boronic acid, (1-methyl-2-naphthalenyl)(9CI), is used as a synthetic intermediate for the creation of complex organic molecules. Its ability to form stable complexes with diols and other hydroxyl-containing compounds facilitates the synthesis of a variety of organic compounds, making it a valuable tool in the field of organic chemistry.
Used in Pharmaceutical Research:
In pharmaceutical research, Boronic acid, (1-methyl-2-naphthalenyl)(9CI), is utilized as a building block for the development of new drugs. Its unique chemical properties, including its reactivity with hydroxyl groups, can be harnessed to design and synthesize pharmaceutically active compounds with potential therapeutic applications.
Used in Material Science:
Boronic acid, (1-methyl-2-naphthalenyl)(9CI), is employed as a component in the development of new materials. Its capacity to form stable complexes can be leveraged to create materials with specific properties, such as improved binding or catalytic capabilities, which can be beneficial in various material science applications.
Used in Chemical Biology:
In chemical biology, Boronic acid, (1-methyl-2-naphthalenyl)(9CI), is used as a probe or modifier of biological systems. Its interactions with biomolecules, such as sugars and glycoproteins, can provide insights into biological processes and be used to develop new tools for studying biological systems.
Each of these applications highlights the versatility and potential of Boronic acid, (1-methyl-2-naphthalenyl)(9CI), in advancing scientific research and technological development across multiple disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 590401-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,0,4,0 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 590401-47:
(8*5)+(7*9)+(6*0)+(5*4)+(4*0)+(3*1)+(2*4)+(1*7)=141
141 % 10 = 1
So 590401-47-1 is a valid CAS Registry Number.
590401-47-1Relevant articles and documents
Synthesis of Phenacene-Helicene Hybrids by Directed Remote Metalation
Kancherla, Sindhu,J?rgensen, K?re B.
supporting information, p. 11140 - 11153 (2020/11/20)
Polycyclic aromatic hydrocarbons (PAHs) with six and seven rings were synthesized via directed metalation and cross-coupling of chrysenyl N,N-diethyl carboxamides with o-tolyl and methylnaphthalenyl derivatives. In the presence of competing ortho sites, the site selectivity in iodination of chrysenyl amides by directed ortho metalation (DoM) was influenced by the lithium base. The catalyst ligand bite angle was presumably important in the cross-coupling of sterically hindered bulky PAHs. Subsequent directed remote metalation of biaryls under standard conditions and at elevated temperatures afforded various fused six- and seven-ring PAHs, all in good yields and with fluorescent properties.
A concise synthesis of novel naphtho[a]carbazoles and benzo[c]carbazoles
Pathak, Rakhi,Nhlapo, Johanna M.,Govender, Sameshnee,Michael, Joseph P.,Van Otterlo, Willem A. L.,De Koning, Charles B.
, p. 2820 - 2830 (2007/10/03)
Starting from simple indole precursors the synthesis of naphtho[a]carbazoles and benzo[c]carbazoles is described. Key steps include the use of the Suzuki-Miyaura reaction to afford 2- or 3-aryl substituted indoles, as well as a potassium t-butoxide and light assisted aromatic ring-forming reaction.
The synthesis of naphtho[a]carbazoles and benzo[c]carbazoles
De Koning, Charles B.,Michael, Joseph P.,Nhlapo, Johanna M.,Pathak, Rakhi,Van Otterlo, Willem A. L.
, p. 705 - 707 (2007/10/03)
The synthesis of naphtho[a]carbazoles and benzo[c]carbazoles from indole precursors using a reaction mediated by potassium t-butoxide and light is described. The indole precursors were prepared utilizing Suzuki coupling methodology.
