34959-81-4 Usage
Uses
Used in Organic Chemistry:
ETHYL 3-CHLORO-2,4-DIOXOPENTANOATE is used as a reagent in organic chemistry for its ability to participate in various chemical reactions due to its ester functional group and the presence of a chlorine atom. This makes it a versatile component in the synthesis of other organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, ETHYL 3-CHLORO-2,4-DIOXOPENTANOATE is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure may contribute to the development of new drugs, potentially enhancing the therapeutic options available for various medical conditions.
Used in Industrial Applications:
Although not explicitly detailed in the provided materials, the potential industrial uses of ETHYL 3-CHLORO-2,4-DIOXOPENTANOATE could be explored further. Its properties might find applications in areas such as material science, where it could be utilized in the development of new materials with specific characteristics.
Further Research and Development:
The properties and potential applications of ETHYL 3-CHLORO-2,4-DIOXOPENTANOATE could be further explored through ongoing research and development. This may lead to the discovery of new uses in various industries, expanding the compound's utility and impact on scientific and technological advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 34959-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,5 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34959-81:
(7*3)+(6*4)+(5*9)+(4*5)+(3*9)+(2*8)+(1*1)=154
154 % 10 = 4
So 34959-81-4 is a valid CAS Registry Number.
34959-81-4Relevant academic research and scientific papers
BI-ARYL DIHYDROOROTATE DEHYDROGENASE INHIBITORS
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Page/Page column 200; 260, (2021/04/17)
Disclosed are compounds, compositions and methods for treating diseases, disorders, or medical conditions that are affected by the modulation of DHODH. Such compounds are represented by Formula I as follows: Formula I wherein R1, R2, R3, and Q are defined herein.
GLYCOLATE OXIDASE INHIBITORS AND USE THEREOF
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Paragraph 0216, (2019/07/17)
The present invention provides pyrazoles, isoxazoles, isothiazoles, thiadiazoles, and pyridazines according to Formula I as described herein, and pharmaceutically acceptable salts thereof. Pharmaceutical compositions and methods for treating primary hyperoxaluria, type I (PH) and kidney stones are also described.
3-(substituted phenyl)-5-(substituted heterocyclyl)-1,2,4-triazole compounds
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, (2008/06/13)
3-(Substituted phenyl)-5-(substituted heterocyclyl)-1,2,4-triazole compounds are useful as insecticides and acaricides. New synthetic procedures and intermediates for preparing the compounds, pesticide compositions containing the compounds, and methods of controlling insects and mites using the compounds are also provided.
One pot synthesis of 1,2,4-triazoles
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, (2008/06/13)
One pot synthesis of 1,2,4-triazoles uses thioimidate intermediate and 1,2-dichloroethane solvent.
