32304-29-3 Usage
Description
(4-Perfluorotolyl)acetic acid, with the molecular formula C9HF13O2, is a perfluorinated carboxylic acid known for its stability and resistance to degradation. It is characterized by its unique chemical structure with multiple perfluorinated groups, which confer high thermal and chemical stability, as well as low surface energy.
Uses
Used in Polymer Synthesis:
(4-Perfluorotolyl)acetic acid is used as a building block in the synthesis of polymers and specialty chemicals, leveraging its high thermal and chemical stability for the creation of advanced materials.
Used in Electronics Industry:
In the electronics industry, (4-Perfluorotolyl)acetic acid is used as a component in the production of materials with high thermal and chemical stability, which are essential for various electronic applications.
Used in Coatings Industry:
(4-Perfluorotolyl)acetic acid is utilized in the coatings industry for its low surface energy, which contributes to the development of coatings with improved durability and resistance to environmental factors.
Environmental and Health Concerns:
Due to its perfluorinated nature, (4-Perfluorotolyl)acetic acid is a potential environmental and health concern. Perfluorinated compounds are known to be persistent and bioaccumulative, which necessitates careful handling and disposal to minimize their impact on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 32304-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32304-29:
(7*3)+(6*2)+(5*3)+(4*0)+(3*4)+(2*2)+(1*9)=73
73 % 10 = 3
So 32304-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H3F7O2/c10-5-2(1-3(17)18)6(11)8(13)4(7(5)12)9(14,15)16/h1H2,(H,17,18)
32304-29-3Relevant articles and documents
Transformations of perfluoroxylenes and perfluoro-p-cymene under the action of Zn(Cu)-DMF-H2O
Krasnov, Vyacheslav I.,Platonov, Vyacheslav E.,Beregovaya, Irina V.,Shchegoleva, Lyudmila N.
, p. 1797 - 1812 (2007/10/03)
Perfluorinated xylenes and perfluoro-para-cymene undergo hydrodefluorination under the action of Zn(Cu)-DMF-H2O. Hydrogen enters mainly at the benzyl position of para-dialkylbenzenes and at the para position to perfluoroalkyl groups of perfluor
