58686-69-4 Usage
Description
(3-TRIFLUOROMETHYL-PHENYL)-PROPYNOIC ACID ETHYL ESTER is an organic compound with the chemical formula C11H11F3O2. It is an ethyl ester of propynoic acid with a trifluoromethyl-substituted phenyl group. (3-TRIFLUOROMETHYL-PHENYL)-PROPYNOIC ACID ETHYL ESTER possesses potential medicinal properties and is of interest in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Research:
(3-TRIFLUOROMETHYL-PHENYL)-PROPYNOIC ACID ETHYL ESTER is used as a compound of interest for its potential applications in the development of new drugs. Its unique structure and properties make it a candidate for further exploration and research in medicinal chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-TRIFLUOROMETHYL-PHENYL)-PROPYNOIC ACID ETHYL ESTER is used for its potential to contribute to the discovery and design of novel therapeutic agents. Its specific characteristics may offer advantages in the treatment of various diseases and conditions, although further research is needed to fully understand its capabilities and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58686-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58686-69:
(7*5)+(6*8)+(5*6)+(4*8)+(3*6)+(2*6)+(1*9)=184
184 % 10 = 4
So 58686-69-4 is a valid CAS Registry Number.
58686-69-4Relevant articles and documents
Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3- azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes
Durham, Robin,Mandel, Jeremie,Blanchard, Nicolas,Tam, William
scheme or table, p. 1494 - 1505 (2012/01/12)
Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3- azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes were investigated. Yields of up to 90% were obtained though regioselectivity was modest. Select cycloadducts could be separated and used to access a highly functionalized [3.2.0] bicyclic structure through reductive cleavage of the N-O bond. These ring-opened products displayed a chemical exchange phenomenon in 1D carbon NMR and required characterization by 2D NMR techniques.