70976-13-5 Usage
Description
(2-TRIFLUOROMETHYL-1,3DIOXOLAN-2-YL)-ACETIC ACID is a synthetic organic compound characterized by the presence of a trifluoromethyl group attached to a dioxolane ring, which is in turn attached to an acetic acid moiety. It has potential applications in the pharmaceutical and agrochemical industries due to its unique chemical structure and potential biological activity.
Used in Pharmaceutical Industry:
(2-TRIFLUOROMETHYL-1,3DIOXOLAN-2-YL)-ACETIC ACID is used as a building block for the synthesis of various pharmacologically active compounds. Its unique chemical structure and potential biological activity make it a promising candidate for the development of new drugs.
Used in Agrochemical Industry:
(2-TRIFLUOROMETHYL-1,3DIOXOLAN-2-YL)-ACETIC ACID is used as a precursor to other organic molecules. Its trifluoromethyl group can confer unique physicochemical properties that make it useful in the development of agrochemicals.
However, further research and testing would be necessary to fully understand the potential uses and properties of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 70976-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,7 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70976-13:
(7*7)+(6*0)+(5*9)+(4*7)+(3*6)+(2*1)+(1*3)=145
145 % 10 = 5
So 70976-13-5 is a valid CAS Registry Number.
70976-13-5Relevant articles and documents
Reactions of polyfluoro-2-alkynoic acids with bifunctional hetero nucleophiles leading to polyfluoroalkylated heterocycles
Yamanaka, Hiroki,Tamura, Kazushige,Funabiki, Kazumasa,Fukunishi, Koushi,Ishihara, Takashi
, p. 177 - 190 (2007/10/02)
Polyfluoro-2-alkynoic acids, Rf-CC-COOH (Rf = HCF2, CF3, H(CF2)3), readily undergo tandem intermolecular-intramolecular Michael addition with bifunctional hetero nucleophiles, HX(CH2)nYH (X, Y = S, O; n = 2, 3), to give 2-polyfluoroalkylated 1,3-diheterocyclic compounds in good to excellent yields.
