1796-12-9 Usage
Uses
Used in Organic Synthesis:
Bromodifluoroacetyl bromide is used as an acylating agent for the modification of organic compounds. Its reactivity allows for the introduction of acyl groups into various organic molecules, facilitating the synthesis of complex organic structures.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, bromodifluoroacetyl bromide is utilized as a key intermediate in the synthesis of various drugs. Its ability to acylate functional groups makes it instrumental in the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
Similarly, in agrochemical production, bromodifluoroacetyl bromide serves as a crucial component in the synthesis of pesticides and other crop protection agents. Its reactivity contributes to the development of effective and novel agrochemicals designed to protect crops from pests and diseases.
Used in Research and Development:
Bromodifluoroacetyl bromide is also employed in research laboratories for the exploration of new chemical reactions and the development of innovative synthetic pathways. Its versatility as a reagent makes it a valuable tool for scientists working on the frontiers of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1796-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1796-12:
(6*1)+(5*7)+(4*9)+(3*6)+(2*1)+(1*2)=99
99 % 10 = 9
So 1796-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C2Br2F2O/c3-1(7)2(4,5)6
1796-12-9Relevant academic research and scientific papers
Production process of ethyl bromodifluoroacetate
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Paragraph 0026, (2020/12/30)
The invention discloses a production process of ethyl bromodifluoroacetate. The production process comprises the following steps: 1, bromination reaction; 2, elimination reaction; 3, oxidation reaction; 4, esterification reaction. Compared with other methods, the bromination addition reaction only needs to be carried out at normal pressure and under the catalysis of infrared light, so that the cost is saved compared with other catalysts, other impurities are not introduced, and the utilization rate of bromine is increased. The elimination reaction adopts a dropwise adding mode, so the reactionrate can be effectively controlled, and the flooding phenomenon which is easy to generate is avoided. The purity of the prepared finished product is greater than or equal to 99.0%, and the yield is greater than or equal to 80.0%.
