136909-72-3 Usage
Uses
Used in Industrial Processes:
4,4,5,5,6,6,6-HEPTAFLUORO-2-HEXANONE is used as a solvent in various industrial processes for its ability to withstand harsh conditions and its effectiveness in dissolving a wide range of substances.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4,4,5,5,6,6,6-HEPTAFLUORO-2-HEXANONE is used as a critical intermediate in the synthesis of certain drugs, leveraging its unique reactivity and stability.
Used in Agrochemical Production:
4,4,5,5,6,6,6-HEPTAFLUORO-2-HEXANONE is utilized in the development of agrochemicals, where its chemical properties contribute to the effectiveness and stability of the final products.
Used in Electronic Materials:
4,4,5,5,6,6,6-HEPTAFLUORO-2-HEXANONE is also employed in the creation of electronic materials, where its resistance to heat and chemicals is advantageous for components that must operate under demanding conditions.
Safety Note:
It is crucial to handle 4,4,5,5,6,6,6-HEPTAFLUORO-2-HEXANONE with care due to its potential to cause irritation to the skin, eyes, and respiratory system if not used properly, emphasizing the need for proper safety measures during its application.
Check Digit Verification of cas no
The CAS Registry Mumber 136909-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136909-72:
(8*1)+(7*3)+(6*6)+(5*9)+(4*0)+(3*9)+(2*7)+(1*2)=153
153 % 10 = 3
So 136909-72-3 is a valid CAS Registry Number.
136909-72-3Relevant articles and documents
ELECTROCHEMICAL SYNTHESIS OF PERFLUOROALKYLACETONES
Vol'pin, I. M.,Kurykin, M. A.,Grinberg, V. A.,Vasil'ev, Yu. B.,German, L. S.
, p. 1395 - 1400 (2007/10/02)
The interaction of electrochemically generated radicals in the electrolysis of the perfluorocarboxylic acids RFCF2COOH (I), where RF = F (a), CF3 (b), C2F5 (c), C3F7 (d), C5F11 (e). and C7F15 (f), with isoprenyl acetate (II) was studied.The dependence of the results of the electrolysis on the adsorption capacity of the anode permits the proposition that the interaction of (II) with the ECG-radicals occurs close to the surface of the electrode.The yield of the perfluoroalkylacetones comprised 30-37percent.