306936-81-2 Usage
Uses
Used in Organic Synthesis:
ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE is used as a reagent in organic synthesis for its high reactivity and ability to undergo various chemical transformations. It aids in the creation of complex organic molecules, making it a crucial component in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE is employed as a key intermediate in the synthesis of potential drug candidates. Its unique structure and reactivity enable the exploration of novel therapeutic agents with improved efficacy and selectivity.
Used in the Development of New Drugs:
ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE has potential applications in the development of new drugs, where its unique properties can be leveraged to design and synthesize innovative pharmaceutical compounds with enhanced therapeutic profiles.
Used in Agrochemicals:
ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE also finds use in the agrochemical industry, where it can be employed as a building block for the synthesis of new agrochemicals, potentially leading to the development of more effective and targeted pest control agents.
Used in Specialty Chemicals:
ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE is utilized in the synthesis of specialty chemicals, where its unique structural features and reactivity can contribute to the creation of high-value chemical products for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 306936-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 306936-81:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*6)+(2*8)+(1*1)=152
152 % 10 = 2
So 306936-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H8F6O3/c1-2-21-10(20)9(19)7-4-3-6(11(13,14)15)5-8(7)12(16,17)18/h3-5H,2H2,1H3
306936-81-2Relevant academic research and scientific papers
The synthesis and structure-activity relationships of 1,3-diaryl 1,2,4-(4H)-triazol-5-ones: A new class of calcium-dependent, large conductance, potassium (maxi-K) channel openers targeted for urge urinary incontinence
Hewawasam, Piyasena,Erway, Matthew,Thalody, George,Weiner, Harvey,Boissard, Christopher G.,Gribkoff, Valentin K.,Meanwell, Nicholas A.,Lodge, Nicholas,Starrett, Jr, John E.
, p. 1117 - 1120 (2007/10/03)
A series of 1,3-diaryl 1,2,4-(4H)-triazol-5-ones was prepared and shown by electrophysiological analysis to activate a cloned maxi-K channel mSlo (or hSlo) expressed in Xenopus laevis oocytes. The effects of these structurally novel maxi-K channel openers on bladder contractile function were studied in vitro using isolated rat bladder strips pre-contracted with carbachol. Several 1,3-diaryl 1,2,4-(4H)-triazol-5-one derivatives were found to be potent smooth muscle relaxants but this activity did not completely correlate with maxi-K channel opening.
