860457-99-4 Usage
Description
Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate is a chemical compound characterized by the molecular formula C11H9F3N2O2. It is a derivative of the heterocyclic compound imidazo[1,2-a]pyridine, which is recognized for its pharmacological activities. This specific compound features an ethyl ester group, a trifluoromethyl group, and a carboxylate group, all of which are significant functional groups in the realm of organic chemistry. Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate's potential applications are primarily in the pharmaceutical industry, where it may contribute to the development of novel drugs or pharmacological agents. The exact properties and uses of this compound are subject to the specific research and development initiatives it is part of.
Uses
Used in Pharmaceutical Industry:
Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate is used as a chemical intermediate for the synthesis of new drugs or pharmacological agents due to its unique structural features and potential pharmacological activities.
Used in Drug Development:
Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate is utilized as a building block in the development of innovative therapeutics, leveraging its functional groups to create molecules with specific biological activities and properties.
Used in Medicinal Chemistry Research:
Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate serves as a subject of study in medicinal chemistry, where its structure-activity relationships are explored to understand its potential interactions with biological targets and its efficacy in treating various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 860457-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,4,5 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 860457-99:
(8*8)+(7*6)+(6*0)+(5*4)+(4*5)+(3*7)+(2*9)+(1*9)=194
194 % 10 = 4
So 860457-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9F3N2O2/c1-2-18-10(17)8-6-16-5-7(11(12,13)14)3-4-9(16)15-8/h3-6H,2H2,1H3
860457-99-4Relevant articles and documents
PESTICIDALLY ACTIVE HETEROCYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS
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Page/Page column 87-89, (2022/03/22)
Compounds of the formula (I) wherein G1, G2, X, R2 and Q are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling animal pests, including arthropods and in particular insects, molluscs, nematodes or representatives of the order Acarina.
NOVEL PHARMACEUTICAL COMPRISING HETEROAROMATIC AMIDE DERIVATIVE OR SALT THEREOF
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Paragraph 0331-0333, (2021/09/17)
PROBLEM TO BE SOLVED: To provide a compound useful for treating or preventing disease associated with voltage-dependent sodium channel (Nav1.7) such as disease involving a pain, disease involving an itch, autonomic nerve-associated disease, or a pharmaceutical composition thereof. SOLUTION: The present disclosure provides a compound illustrated by the following formula, and a pharmaceutical composition containing the same. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT
The discovery of fluazaindolizine: A new product for the control of plant parasitic nematodes
Lahm, George P.,Desaeger, Johan,Smith, Ben K.,Pahutski, Thomas F.,Rivera, Michel A.,Meloro, Tony,Kucharczyk, Roman,Lett, Renee M.,Daly, Anne,Smith, Brenton T.,Cordova, Daniel,Thoden, Tim,Wiles, John A.
, p. 1572 - 1575 (2017/03/17)
Fluazaindolizine is a new highly effective and selective product for the control of plant parasitic nematodes. Specificity for nematodes coupled with absence of activity against the target sites of commercial nematicides suggests that fluazaindolizine has a novel mode of action. The discovery, structure-activity development and biological properties for this new class of nematicides are presented.