353-99-1 Usage
Uses
1. Used in Chemical Synthesis:
DIBROMOFLUOROACETIC ACID is used as a reagent in various chemical synthesis processes for the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique properties allow for the formation of specific chemical bonds and reactions that are not possible with other compounds.
2. Used in Laboratory Research:
In the field of laboratory research, DIBROMOFLUOROACETIC ACID is utilized as a tool to study various biological and chemical phenomena. Its ability to interact with specific proteins and enzymes makes it a valuable research compound for understanding the mechanisms of action and potential applications in drug development.
3. Used in Industrial Processes:
DIBROMOFLUOROACETIC ACID is employed in certain industrial processes, such as the manufacturing of dyes, plastics, and other chemical products. Its strong acidic nature and reactivity contribute to the production of desired end products in these industries.
4. Used in Environmental Remediation:
Despite its potential environmental hazards, DIBROMOFLUOROACETIC ACID can also be used in environmental remediation efforts. It can be employed to neutralize or break down other harmful chemicals in contaminated soil or water sources, thereby mitigating their negative impact on the environment.
5. Used in Analytical Chemistry:
In analytical chemistry, DIBROMOFLUOROACETIC ACID serves as a titrant or standard solution for the determination of various chemical properties and concentrations. Its strong acidic nature and precise molar mass make it suitable for accurate measurements and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 353-99-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 353-99:
(5*3)+(4*5)+(3*3)+(2*9)+(1*9)=71
71 % 10 = 1
So 353-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C2HBr2FO2/c3-2(4,5)1(6)7/h(H,6,7)
353-99-1Relevant academic research and scientific papers
One-step synthesis of highly functionalized monofluorinated cyclopropanes from electron-deficient alkenes
Ivashkin, Pavel,Couve-Bonnaire, Samuel,Jubault, Philippe,Pannecoucke, Xavier
supporting information; experimental part, p. 2270 - 2273 (2012/06/18)
The unique combination of Zn/LiCl allowed generation of reactive zinc enolate from ethyl dibromofluoroacetate. This fluorinated enolate reacts efficiently with a wide range of functionalized electron-deficient alkenes to afford the corresponding monofluorinated cyclopropylcarboxylates in good yields.
Asymmetric synthesis of cyclopropanes with a monofluorinated quaternary stereocenter
Ivashkin, Pavel,Couve-Bonnaire, Samuel,Jubault, Philippe,Pannecoucke, Xavier
supporting information, p. 5130 - 5133 (2013/01/15)
New chiral fluorinated reagents (N-(dibromofluoroacetyl)oxazolidinones) were easily synthesized and used in an asymmetric cyclopropanation process. The Michael initiated ring closure reaction provided chiral cyclopropanes bearing a fluorinated quaternary stereocenter. Various electron-deficient alkenes can be used to efficiently obtain chiral polysubtituted fluorinated cyclopropanes in good yields. Moderate to very good cis/trans ratios were obtained with a high level of diastereoselectivity for each isomer.
