29553-26-2 Usage
Uses
Used in Pharmaceutical Industry:
2,2,3,3-Tetrafluoro-1,1-dimethylpropanol is utilized as a solvent and intermediate for the synthesis of various pharmaceutical compounds. Its unique properties contribute to the development of new drugs and the improvement of existing ones, enhancing their efficacy and safety.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,3,3-tetrafluoro-1,1-dimethylpropanol is employed as a key component in the production of pesticides and other agrochemicals. Its role in these applications is to improve the performance and environmental compatibility of these products.
Used as a Solvent:
2,2,3,3-Tetrafluoro-1,1-dimethylpropanol is used as a solvent in various industrial processes due to its ability to dissolve a wide range of substances. Its non-flammable nature makes it a safer alternative to traditional solvents, reducing the risk of accidents and fires.
Used as a Surfactant:
2,2,3,3-TETRAFLUORO-1,1-DIMETHYLPROPANOL also serves as a surfactant, which is essential in the formulation of products that require stable dispersions or emulsions. Its surfactant properties contribute to the improved performance and stability of these products.
Used in the Production of Industrial Products:
2,2,3,3-Tetrafluoro-1,1-dimethylpropanol is an important intermediate in the manufacturing of a variety of industrial products, including fluoropolymers, which are known for their exceptional chemical resistance and thermal stability. Its presence in these products enhances their performance and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 29553-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29553-26:
(7*2)+(6*9)+(5*5)+(4*5)+(3*3)+(2*2)+(1*6)=132
132 % 10 = 2
So 29553-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H8F4O/c1-4(2,10)5(8,9)3(6)7/h3,10H,1-2H3
29553-26-2Relevant academic research and scientific papers
Promising prospects for using partially fluorinated alcohols as O-nucleophilic reagents in organofluoric synthesis
Il'in,Il'in,Bakhmutov,Furin,Pokrovskii
, p. 405 - 418 (2008/02/02)
Perfluoroolefins react with isopropyl alcohol under the conditions of radical initiation to form partially fluorinated aliphatic alcohols. The reactions of these alcohols with hexafluoropropylene and compounds containing labile halogen atoms (in particular, with allyl bromide and epichlorohydrin) were studied.
PHOTOCHEMICAL SYNTHESIS OF FLUOROALKANOLS BASED ON TETRAFLUOROETHYLENE
Paleta, O.,Dedek, V.,Reutschek, H.,Timpe, H.-J.
, p. 345 - 354 (2007/10/02)
The conditions of the photochemical synthesis of fluoroalkanols H(C2F4)nC(OH)R1R2 (n = 1, 2) by the reaction of tetrafluoroethylene with alcohols in the presence of photoinitiators and sensitisers are described.The reaction is initiated by UV radiation and is performed under atmospheric pressure.The yields of alkanols were 0.1-0.39 mol using 250 W UV lamp after 6-8 hours and 73-82 percent relatively to the converted tetrafluoroethylene.
