431-22-1 Usage
Uses
Used in Chemical Industry:
1,2-DIBROMO-3,3,3-TRIFLUOROPROPENE is used as an intermediate for the production of other chemicals, leveraging its unique chemical properties to facilitate the synthesis of a variety of compounds.
Used in Refrigeration Industry:
DBTFP is utilized as a refrigerant due to its thermodynamic properties, which make it suitable for cooling applications in various systems.
Used in Solvent Applications:
As a solvent, 1,2-DIBROMO-3,3,3-TRIFLUOROPROPENE is employed in various industrial processes to dissolve or suspend other substances, taking advantage of its solvency characteristics.
Safety Measures:
When handling 1,2-DIBROMO-3,3,3-TRIFLUOROPROPENE, it is crucial to implement safety protocols to mitigate its flammability and toxicity. This includes the use of protective equipment such as gloves, goggles, and respirators, as well as ensuring that the work environment is well-ventilated to prevent the buildup of harmful vapors. Additionally, due to its potential to react with strong oxidizers, it should be stored and used away from such agents to prevent hazardous reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 431-22-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 431-22:
(5*4)+(4*3)+(3*1)+(2*2)+(1*2)=41
41 % 10 = 1
So 431-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C3HBr2F3/c4-1-2(5)3(6,7)8/h1H
431-22-1Relevant articles and documents
Synthesis of ethyl 3,3,3-trifluoropropionate from 2-bromo-3,3,3-trifluoropropene Dedicated to Dr. Teruo Umemoto on the occasion of his receipt of the ACS Award for Creative Work in Fluorine Chemistry 2014.
Inoue, Munenori,Shiosaki, Masahiro,Muramaru, Hajime
, p. 135 - 138 (2015/03/04)
A facile synthesis of ethyl 3,3,3-trifluoropropionate is described. Commercially available 2-bromo-3,3,3-trifluoropropene was used as a starting material, which was allowed to react with bromine to produce 2,2,3-tribromo-1,1,1-trifluoropropane. The resulting tribromide was treated with 3 equiv. of potassium ethoxide, giving rise to ethyl 3,3,3-trifluoropropionate in 60% overall yield in 2 steps. The reaction proceeded via an alkoxide-induced tandem reaction mechanism.