174884-21-0 Usage
Description
4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester is a white solid compound with a complex chemical structure. It is characterized by its ester functional group and the presence of an acetyl and methoxy group on the phenoxy moiety. This molecule is known for its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester is used as a photolabile linker for the solid-phase synthesis of 4-substituted 1,2,3-triazoles. This application is significant because it allows for the efficient and controlled synthesis of these biologically active compounds, which have been widely explored for their potential use in drug development.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester serves as a versatile building block for the creation of more complex molecules. Its unique structure and functional groups make it a valuable component in the synthesis of various organic compounds, potentially leading to the development of new materials and pharmaceuticals.
Used in Research and Development:
Due to its unique chemical properties, 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester is also used in research and development for studying the reactivity and behavior of ester-containing compounds. This can provide valuable insights into the design and synthesis of new molecules with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 174884-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,8 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174884-21:
(8*1)+(7*7)+(6*4)+(5*8)+(4*8)+(3*4)+(2*2)+(1*1)=170
170 % 10 = 0
So 174884-21-0 is a valid CAS Registry Number.
174884-21-0Relevant articles and documents
PHOTOPROXIMITY PROFILING OF PROTEIN-PROTEIN INTERACTIONS IN CELLS
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Page/Page column 73; 75, (2021/04/01)
Photoactive probes and probe systems for detecting biological interactions are described. The photoactive probes include probes that combine both photocleavable and photoreactive moieties. The photoactive probe systems can include a first probe comprising a photocatalytic group and a second probe comprising a group that can act as a substrate for the reaction catalyzed by the photocatalytic group. The probes and probe systems can also include groups that can specifically bind to a binding partner on a biological entity of interest and a detectable group or a precursor thereof. The probes and probe systems can detect spatiotemporal interactions of proteins or cells. In some embodiments, the interactions can be detected in live cells. Also described are methods of detecting the biological interactions.
PEG-PEI-modified gated N-doped mesoporous carbon nanospheres for pH/NIR light-triggered drug release and cancer phototherapy
Panda, Snigdharani,Bhol, Chandra Sekhar,Bhutia, Sujit Kumar,Mohapatra, Sasmita
, p. 3666 - 3676 (2021/05/17)
A novel hybrid drug carrier has been designed, taking N-doped mesoporous carbon (NMCS) as the core and PEG-PEI as the outer shell. NMCS was functionalized with a photocleavable nitrobenzyl-based linker following a click reaction. Gemcitabine was loaded in
Two Colour Photoflow Chemistry for Macromolecular Design
Barner-Kowollik, Christopher,Blinco, James P.,De Bruycker, Kevin,Van De Walle, Matthias
supporting information, p. 14143 - 14147 (2020/06/10)
We report a photochemical flow setup that exploits λ-orthogonal reactions using two different colours of light (λ1=350 nm and λ2=410 nm) in sequential on-line irradiation steps. Critically, both photochemically reactive units (a visi
