88796-28-5 Usage
Uses
Given the limited information provided, the following potential uses are speculative and based on the compound's chemical structure:
Used in Pharmaceutical Industry:
5-Amino-3-methyl-2-thiophenecarboxylic acid ethyl ester could be used as an intermediate in the synthesis of pharmaceutical compounds for [application reason], due to its unique functional groups that may allow for further chemical reactions and modifications.
Used in Chemical Research:
In the field of chemical research, 5-Amino-3-methyl-2-thiophenecarboxylic acid ethyl ester might serve as a subject for studying the properties and reactivity of Thiophene derivatives, potentially leading to new insights or applications in organic chemistry.
Used in Material Science:
5-Amino-3-methyl-2-thiophenecarboxylic acid ethyl ester could be explored for its potential in the development of new materials, such as polymers or composites, where its Thiophene ring and functional groups may impart specific characteristics to the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 88796-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88796-28:
(7*8)+(6*8)+(5*7)+(4*9)+(3*6)+(2*2)+(1*8)=205
205 % 10 = 5
So 88796-28-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO2S/c1-3-11-8(10)7-5(2)4-6(9)12-7/h4H,3,9H2,1-2H3
88796-28-5Relevant academic research and scientific papers
Bioisosteric approach to the discovery of imidazo[1,2-a]pyrazines as potent Aurora kinase inhibitors
Meng, Zhaoyang,Kulkarni, Bheemashankar A.,Kerekes, Angela D.,Mandal, Amit K.,Esposite, Sara J.,Belanger, David B.,Reddy, Panduranga Adulla,Basso, Andrea D.,Tevar, Seema,Gray, Kimberly,Jones, Jennifer,Smith, Elizabeth B.,Doll, Ronald J.,Siddiqui, M. Arshad
scheme or table, p. 592 - 598 (2011/02/26)
Our continued effort toward the development of the imidazo[1,2-a]pyrazine scaffold as Aurora kinase inhibitors is described. Bioisosteric approach was applied to optimize the 8-position of the core. Several new potent Aurora A/B dual inhibitors, such as 25k and 25l, were identified.
ORGANIC COMPOUNDS
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Page/Page column 94-95, (2008/12/08)
The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.
