90401-87-9 Usage
Uses
Used in Pharmaceutical Research:
2,2,2-Trifluoro-N-(5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)acetamide is used as a building block for the synthesis of various drug candidates. Its unique structure and fluoro-substituted moieties contribute to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Research:
In the agrochemical industry, 2,2,2-trifluoro-N-(5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)acetamide is used as a building block for the synthesis of pesticides. Its chemical properties allow for the creation of novel agrochemicals that can be more effective in controlling pests and diseases in agriculture.
Used in Medicinal Chemistry:
2,2,2-Trifluoro-N-(5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)acetamide is employed as a valuable tool in medicinal chemistry for the design and synthesis of new compounds with potential therapeutic effects. Its unique structure and fluorination can lead to the discovery of new drugs with improved pharmacological properties.
Used in Drug Discovery:
As a promising candidate for drug design, 2,2,2-trifluoro-N-(5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)acetamide is used in drug discovery processes to explore its potential biological activity and pharmacological properties. This can lead to the development of new drugs with novel mechanisms of action and therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 90401-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,0 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90401-87:
(7*9)+(6*0)+(5*4)+(4*0)+(3*1)+(2*8)+(1*7)=109
109 % 10 = 9
So 90401-87-9 is a valid CAS Registry Number.
90401-87-9Relevant academic research and scientific papers
Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors
Onda, Kenichi,Shiraki, Ryota,Ogiyama, Takashi,Yokoyama, Kazuhiro,Momose, Kazuhiro,Katayama, Naoko,Orita, Masaya,Yamaguchi, Tomohiko,Furutani, Masako,Hamada, Noritaka,Takeuchi, Makoto,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-ichi
experimental part, p. 10001 - 10012 (2009/04/06)
As a result of the various N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives with a hydroxy moiety synthesized in an effort to discover novel glycogen phosphorylase (GP) inhibitors, 5-chloro-N-(5-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-1H-indole-2
4,5-DIHYDRONAPHTHO [1,2-b] THIOPHENE DERIVATIVE
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Page/Page column 18, (2010/11/08)
A 4,5-dihydronaphtho[1,2-b]thiophene derivative expressed by the formula: (wherein R1 is a C1 to C10 1-hydroxyalkyl group or a C1 to C10 acyl group, and R2 and R3 separately substitute in the 6-, 7-, 8-, or 9-positions, and are each independently a hydrogen atom, a halogen atom, a C1 to C10 alkyl group, a hydroxy group, a C1 to C10 alkoxy group, a C1 to C5 alkenyloxy group, a C1 to C5 alkynyloxy group, a benzyloxy group, or the like, provided that when R1 is an acyl group and R2 is a hydrogen atom, then R3 is neither a hydrogen atom nor an acetyl group), or a pharmaceutically acceptable salt thereof. This is a novel compound that is effective in reducing triglyceride levels in the liver and reducing blood glucose levels.
