708-84-9 Usage
Uses
Used in Organic Synthesis:
(2Z)-2-fluoro-3-phenylbut-2-enoic acid is used as a building block in organic synthesis for creating more complex organic molecules with potential pharmaceutical applications. Its structural features, including the phenyl group and double bond, contribute to its versatility in forming various molecular structures.
Used in Pharmaceutical Research:
(2Z)-2-fluoro-3-phenylbut-2-enoic acid is used as a starting material in pharmaceutical research for the development of novel molecules with biological activity. Its reactivity and structural features make it a promising candidate for creating new compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
(2Z)-2-fluoro-3-phenylbut-2-enoic acid is used as a key intermediate in the synthesis of fluorinated compounds for medicinal purposes. The presence of the fluorine atom in its structure endows it with unique properties that can be exploited in the development of new drugs with improved pharmacokinetics and pharmacodynamics.
Used in Agrochemical Development:
(2Z)-2-fluoro-3-phenylbut-2-enoic acid is also used in the development of fluorinated compounds for agrochemical purposes. Its potential applications in this field include the creation of new pesticides, herbicides, and other agrochemicals with enhanced efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 708-84-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 708-84:
(5*7)+(4*0)+(3*8)+(2*8)+(1*4)=79
79 % 10 = 9
So 708-84-9 is a valid CAS Registry Number.
708-84-9Relevant academic research and scientific papers
On the reactions of trifluorovinylsilanes with aromatic ketones - Expected and some unexpected results
Kirij,Dontsova,Pavlenko,Yagupolskii,Tyrra,Naumann
scheme or table, p. 184 - 189 (2010/04/30)
The reactions of aromatic ketones with trialkyl(trifluorovinyl)silanes in the presence of fluoride ions were studied. The conditions for the selective addition of trialkyl(trifluorovinyl)silanes to the carbonyl function of aromatic ketones in the presence
