17425-25-1 Usage
Uses
Used in Pharmaceutical Production:
3,3,4,4-Tetrafluorobutan-2-ol serves as a crucial intermediate in the synthesis of various pharmaceuticals, leveraging its unique fluorinated structure to enhance the properties of the final drug products.
Used in Agrochemicals:
In the agrochemical industry, 3,3,4,4-Tetrafluorobutan-2-ol is utilized as a key component in the development of effective and targeted pesticides and other agricultural chemicals, contributing to improved crop protection and yield.
Used in Specialty Chemicals:
3,3,4,4-Tetrafluorobutan-2-ol is employed in the production of specialty chemicals, where its fluorinated nature imparts specific characteristics that are beneficial for various industrial applications.
Used as a Solvent in Organic Synthesis:
3,3,4,4-Tetrafluorobutan-2-ol also functions as a solvent in organic synthesis processes, providing a medium for chemical reactions to occur, particularly in reactions involving fluorinated compounds. Its properties may facilitate or enhance the reaction outcomes in certain cases.
Check Digit Verification of cas no
The CAS Registry Mumber 17425-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,2 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17425-25:
(7*1)+(6*7)+(5*4)+(4*2)+(3*5)+(2*2)+(1*5)=101
101 % 10 = 1
So 17425-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H6F4O/c1-2(9)4(7,8)3(5)6/h2-3,9H,1H3
17425-25-1Relevant academic research and scientific papers
Il'in,Il'in,Bakhmutov,Furin,Pokrovskii
, p. 405 - 418 (2007)
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.
