180918-40-5 Usage
Description
3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is a colorless, odorless liquid chemical compound with the molecular formula C6H9F3O2. It is characterized by its high stability and resistance to hydrolysis, making it a valuable building block for the synthesis of other fluorinated compounds. Its unique chemical structure also offers potential applications in various fields, including pharmaceuticals, agrochemicals, materials science, and the production of fluorinated compounds.
Uses
Used in Pharmaceutical Industry:
3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique properties and high stability make it suitable for the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical industry, 3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used as a building block for the synthesis of various agrochemicals, including pesticides and herbicides. Its resistance to hydrolysis and high stability contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Production of Fluorinated Compounds:
3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used as a starting material for the production of various fluorinated compounds. Its unique chemical structure allows for the creation of new compounds with enhanced properties, such as increased thermal stability, chemical resistance, and improved performance in specific applications.
Used as a Solvent:
Due to its chemical properties, 3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used as a solvent in various chemical processes. Its ability to dissolve a wide range of substances and its compatibility with different materials make it a versatile solvent for various applications.
Used as a Reagent in Organic Synthesis:
3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used as a reagent in organic synthesis, enabling the formation of new chemical compounds and facilitating various chemical reactions. Its unique properties and reactivity contribute to the development of novel synthetic routes and the production of new organic compounds.
Used in Materials Science:
In the field of materials science, 3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is used in the development of fluorinated polymers and coatings. Its unique chemical structure and properties allow for the creation of materials with enhanced performance characteristics, such as increased durability, chemical resistance, and improved thermal stability.
Overall, 3,3,3-TRIFLUORO-2,2-DIMETHYLPROPIONIC ACID is a versatile chemical compound with a wide range of applications across various industries, making it an essential component in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 180918-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,9,1 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 180918-40:
(8*1)+(7*8)+(6*0)+(5*9)+(4*1)+(3*8)+(2*4)+(1*0)=145
145 % 10 = 5
So 180918-40-5 is a valid CAS Registry Number.
180918-40-5Relevant articles and documents
Selective reactions of 1,1-cycloalkanedicarboxylic acids with SF4. a route to 1,1-bis(trifluoromethyl)cycloalkanes, 1-fluoroformyl-1-(trifluoromethyl)cycloalkanes and 1-(trifluoromethyl)-1-cycloalkanecarboxylic acids
Dmowski, Wojciech,Wolniewicz, Adam
, p. 141 - 146 (2007/10/03)
Six-, five-, four- and three-membered 1,1-cycloalkanedicarboxylic acid (2a-d) were synthesized by alkaline hydrolysis of the corresponding diesters (1a-d) and the reactions of the formers with SF4 were investigated. 1,1-Bis(trifluoromethyl)cycloalkanes (3a-d) were the products of the reactions conducted at 120-150°C while at 30°C 1-fluoroformyl-1-(trifluoromethyl)cycloalkanes (4a-d) were exclusively formed. The latter were isolated as pure compounds or converted in situ into 1-(trifluoromethyl)-1-cycloalkanecarboxylic acids (5a-d).