824983-56-4 Usage
Uses
Used in Pharmaceutical Synthesis:
5-Fluoro-2-thiopheneMethanol serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 5-Fluoro-2-thiopheneMethanol is utilized for the production of a range of agrochemicals. Its incorporation in these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used as a Building Block in Organic Chemistry:
5-Fluoro-2-thiopheneMethanol also functions as a valuable building block in organic chemistry. Its presence in chemical reactions can lead to the creation of a diverse array of organic compounds, expanding the horizons of synthetic organic chemistry.
Used in Chemical Research and Development:
Due to its unique chemical properties, 5-Fluoro-2-thiopheneMethanol is a compound of interest for chemical research and development. It is employed in various studies to explore new reactions, mechanisms, and potential applications, thereby contributing to the innovation in the chemical sciences.
Used in Industrial Applications:
5-Fluoro-2-thiopheneMethanol finds its place in numerous industrial applications, where it is utilized in the production of a wide range of products. Its versatility and reactivity make it an indispensable component in various industrial processes and final products.
Check Digit Verification of cas no
The CAS Registry Mumber 824983-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 824983-56:
(8*8)+(7*2)+(6*4)+(5*9)+(4*8)+(3*3)+(2*5)+(1*6)=204
204 % 10 = 4
So 824983-56-4 is a valid CAS Registry Number.
824983-56-4Relevant academic research and scientific papers
FLUORO-SUBSTITUTED INHIBITORS OF D-AMINO ACID OXIDASE
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Page/Page column 30-31, (2008/06/13)
This invention provides novel inhibitors of the enzyme D-amino acid oxidase as well as pharmaceutical compositions including the compounds of the invention. The invention also provides methods for the treatment and prevention of neurological disorders, such as neuropsychiatric and neurodegenerative diseases, as well as pain, ataxia and convulsion. The compounds of the invention have the general structure: wherein A is NH or S. Q is a member selected from CR1 and N. X and Y are members independently selected from O, S, CR2, N and NH. R1, R2 and R4 are members independently selected from H and F, provided that at least one member selected from R1, R2 and R4 is F. R6 is a member selected from O?X+ and OH, wherein X+ is a positive ion, which is a member selected from inorganic positive ions and organic positive ions.
