455-72-1 Usage
Description
(3-fluoro-4-methoxy-phenyl)-glyoxylic acid is a chemical compound that features a unique combination of a fluoro, methoxy, and phenyl group attached to a glyoxylic acid moiety. This distinct chemical structure and properties may offer potential applications in organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
(3-fluoro-4-methoxy-phenyl)-glyoxylic acid is used as a building block for the synthesis of complex molecules, due to its distinct chemical structure and properties.
Used in Pharmaceutical Research:
(3-fluoro-4-methoxy-phenyl)-glyoxylic acid is used as a potential drug candidate, given its unique chemical structure and properties that may be of interest for further study and potential applications in various fields.
Used in Research and Development:
The fluoro and methoxy substituents in (3-fluoro-4-methoxy-phenyl)-glyoxylic acid may impart unique properties to the compound, making it a valuable subject for research and development in various scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 455-72-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 455-72:
(5*4)+(4*5)+(3*5)+(2*7)+(1*2)=71
71 % 10 = 1
So 455-72-1 is a valid CAS Registry Number.
455-72-1Relevant articles and documents
Visible-Light-Triggered, Metal- and Photocatalyst-Free Acylation of N-Heterocycles
Guillemard, Lucas,Colobert, Fran?oise,Wencel-Delord, Joanna
, p. 4184 - 4190 (2018)
A photoinduced acylation of N-heterocycles is explored. This visible-light triggered reaction occurs not only under extremely mild reaction conditions, but also does not require the presence of a photosensitizer. The mechanistic studies suggest formation of EDA complexes prompt to harness the energy from visible-light. Compatibility with a large panel of α-keto acids as acyl precursors and an array of N-heterocycles clearly showcase the synthetic potential of this handy and green acylation protocol. (Figure presented.).
