259796-12-8 Usage
Description
3,5-dichloro-N-Methoxy-N-MethylbenzaMide is a chemical compound with the molecular formula C9H10Cl2NO2. It is a white solid crystalline substance that is soluble in organic solvents. 3,5-dichloro-N-Methoxy-N-MethylbenzaMide is commonly used in organic synthesis and pharmaceutical research as a building block for the development of various drugs and biologically active compounds. It has also been studied for its potential applications in the treatment of certain diseases and conditions. Additionally, it is known for its mild analgesic and anti-inflammatory properties, making it a candidate for further pharmaceutical development. Overall, 3,5-dichloro-N-methoxy-N-methylbenzamide is a valuable chemical with potential applications in medicinal and research fields.
Uses
Used in Pharmaceutical Research:
3,5-dichloro-N-Methoxy-N-MethylbenzaMide is used as a building block in pharmaceutical research for the development of various drugs and biologically active compounds. Its unique chemical structure allows it to be a versatile component in the synthesis of new molecules with potential therapeutic applications.
Used in Organic Synthesis:
3,5-dichloro-N-Methoxy-N-MethylbenzaMide is used as a key intermediate in organic synthesis, enabling the creation of a wide range of chemical compounds. Its reactivity and functional groups make it a valuable component in the synthesis of complex organic molecules.
Used in Disease Treatment Research:
3,5-dichloro-N-Methoxy-N-MethylbenzaMide is used in research aimed at developing treatments for certain diseases and conditions. Its potential applications in this area are still under investigation, but its unique properties make it a promising candidate for further study.
Used in Analgesic and Anti-Inflammatory Drug Development:
3,5-dichloro-N-Methoxy-N-MethylbenzaMide is used as a candidate for the development of analgesic and anti-inflammatory drugs due to its mild analgesic and anti-inflammatory properties. Its potential in this area is currently being explored for the creation of new medications to treat pain and inflammation.
Check Digit Verification of cas no
The CAS Registry Mumber 259796-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,7,9 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 259796-12:
(8*2)+(7*5)+(6*9)+(5*7)+(4*9)+(3*6)+(2*1)+(1*2)=198
198 % 10 = 8
So 259796-12-8 is a valid CAS Registry Number.
259796-12-8Relevant articles and documents
Preparation method of 5, 7-dichloro-1, 2, 3, 4-tetrahydroisoquinoline
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Paragraph 0019-0020; 0026-0029; 0039-0041, (2021/02/06)
The invention provides a preparation method of 5, 7-dichloro-1, 2, 3, 4-tetrahydroisoquinoline. The preparation method comprises the following steps: preparing a compound A by taking 3, 5-dichlorobenzoic acid as a raw material; preparing a compound B from the compound A; preparing a compound C from the compound B; preparing a compound D from the compound C; and obtaining a white solid 5, 7-dichloro-1, 2, 3, 4-tetrahydroisoquinoline from the compound D. The preparation method of 5, 7-dichloro-1, 2, 3, 4-tetrahydroisoquinoline provided by the invention has the advantages of high product purity and high product yield.
Design, synthesis, and biological evaluation of potent thiosemicarbazone based cathepsin L inhibitors
Kishore Kumar,Chavarria, Gustavo E.,Charlton-Sevcik, Amanda K.,Arispe, Wara M.,MacDonough, Matthew T.,Strecker, Tracy E.,Chen, Shen-En,Siim, Bronwyn G.,Chaplin, David J.,Trawick, Mary Lynn,Pinney, Kevin G.
supporting information; experimental part, p. 1415 - 1419 (2010/07/06)
A small library of 36 functionalized benzophenone thiosemicarbazone analogs has been prepared by chemical synthesis and evaluated for their ability to inhibit the cysteine proteases cathepsin L and cathepsin B. Inhibitors of cathepsins L and B have the potential to limit or arrest cancer metastasis. The six most active inhibitors of cathepsin L (IC50 50 > 10,000 nM). The most active analog in the series, 3-bromophenyl-2′-fluorophenyl thiosemicarbazone 1, also efficiently inhibits cell invasion of the DU-145 human prostate cancer cell line.
SUBSTITUTED PYRAZOLES, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF USE
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Page/Page column 32, (2008/06/13)
The present invention relates to substituted pyrazoles, compositions containing such compounds and methods of treatment. The compounds are glucagon receptor antagonists and thus are useful for treating, preventing or delaying the onset of type 2 diabetes
