204707-42-6 Usage
Description
4-fluoro-2-methoxybenzoic acid methyl ester, also known as Methyl 4-fluoro-2-methoxybenzoate, is an organic compound derived from the esterification of 4-fluoro-2-methoxybenzoic acid with methanol. It is characterized by its aromatic structure and functional groups, which contribute to its diverse applications in various industries.
Uses
Used in Pharmaceutical Industry:
4-fluoro-2-methoxybenzoic acid methyl ester is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows it to serve as a building block in the development of new medications, particularly those targeting specific biological pathways.
Used in Catalyst Applications:
In the field of chemistry, 4-fluoro-2-methoxybenzoic acid methyl ester is utilized as a catalyst to accelerate chemical reactions. Its ability to interact with other molecules and facilitate reaction rates makes it a valuable component in various chemical processes.
Used in Kinase Inhibitors:
4-fluoro-2-methoxybenzoic acid methyl ester is also employed in the development of kinase inhibitors, which are essential in the treatment of various diseases, including cancer. Kinase inhibitors work by blocking the activity of specific enzymes, thus disrupting the signaling pathways that promote cell growth and division.
Check Digit Verification of cas no
The CAS Registry Mumber 204707-42-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,7,0 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 204707-42:
(8*2)+(7*0)+(6*4)+(5*7)+(4*0)+(3*7)+(2*4)+(1*2)=106
106 % 10 = 6
So 204707-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9FO3/c1-12-8-5-6(10)3-4-7(8)9(11)13-2/h3-5H,1-2H3
204707-42-6Relevant articles and documents
Fluorinations of unsymmetrical diaryliodonium salts containing: Ortho -sidearms; Influence of sidearm on selectivity
Abudken, Ahmed M. H.,Hope, Eric G.,Singh, Kuldip,Stuart, Alison M.
, p. 6140 - 6146 (2020/10/30)
Activated aromatics were reacted with two different fluoroidoane reagents 1 and 2 in the presence of triflic acid to prepare only the para-substituted diaryliodonium salts. With fluoroiodane 1 the unsymmetrical diaryliodonium salts contained an ortho-propan-2-ol sidearm, whereas the alcohol sidearm was eliminated to form an ortho-styrene sidearm in the reaction with fluoroiodane 2. Only the diaryliodonium salts containing a styrene sidearm were fluorinated successfully to deliver para-fluorinated aromatics in good yields.
Pyrazolo [3,4 - the b] pyridine and [...] composition preparation method and use of (by machine translation)
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Paragraph 0534; 0535; 0536; 0537, (2017/07/22)
The present invention provides a pyrazolo [3,4 - the b] pyridine and [...] compound of preparation and use, in particular, the present invention provides a following formula (I) compounds are shown, wherein the definition of each group as described in the specification. The compounds of the invention has excellent tyrosine kinase inhibiting activity, so can be used for preparing a series of treating diseases associated with the tyrosine kinase activity of the drug. (by machine translation)
Modulators of methyl modifying enzymes, compositions and uses thereof
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Page/Page column 135; 136, (2015/12/26)
Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein.
