459215-46-4 Usage
Uses
Used in Organic Synthesis:
(5-(benzyloxy)-2-fluorophenyl)methano is used as an intermediate in the synthesis of more complex organic molecules. Its unique structure allows for various chemical reactions, making it a valuable building block in the creation of novel compounds with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (5-(benzyloxy)-2-fluorophenyl)methano is used as a key component in the development of new drugs. Its fluorinated nature and the presence of the benzyloxy group may contribute to the compound's bioactivity, potentially leading to the discovery of new therapeutic agents.
Used in Materials Science:
(5-(benzyloxy)-2-fluorophenyl)methano is also utilized in materials science for the development of new materials with specific properties. (5-(benzyloxy)-2-fluorophenyl)methano's molecular structure may be exploited to create materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 459215-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,2,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 459215-46:
(8*4)+(7*5)+(6*9)+(5*2)+(4*1)+(3*5)+(2*4)+(1*6)=164
164 % 10 = 4
So 459215-46-4 is a valid CAS Registry Number.
459215-46-4Relevant academic research and scientific papers
Fused pyrimidine derivatives substituted with a nitrogen-containing heterocyclic ring and their pharmaceutical use
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Paragraph 0525-0526; 0531-0533, (2021/07/17)
The present application relates to fused pyrimidine derivatives substituted with heterocycles containing nitrogen and to their medicinal use. Provided are a compound represented by chemical formula I, a solvate, a stereoisomer thereof, a pharmaceutically
Syntheses of 6-fluoro-meta-tyrosine and of its metabolites
Konkel, Jamie T,Fan, Junfa,Jayachandran,Kirk, Kenneth L
, p. 27 - 32 (2007/10/03)
6-Fluoro-meta-tyrosine (1) was prepared from 2-fluoro-5-hydroxybenzaldehyde (6) based on an Erlenmeyer-Pl?chl azlactone strategy. Products of expected metabolism of the amino acid, including 6-fluoro-meta-tyramine (2) and its O-sulfate conjugate (3), (2-f
