111773-24-1 Usage
Uses
Used in Pharmaceutical Production:
Ethyl 3-bromo-2,2-difluoropropionate serves as an intermediate in the synthesis of various pharmaceuticals. Its unique structure facilitates the creation of new compounds with potential therapeutic applications, contributing to the development of novel medications.
Used in Agrochemical Production:
In the agrochemical industry, Ethyl 3-bromo-2,2-difluoropropionate is utilized as a precursor for the production of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Organic Synthesis:
As a building block in organic synthesis, Ethyl 3-bromo-2,2-difluoropropionate is employed for the construction of complex organic molecules. Its ability to undergo multiple functional group transformations makes it a valuable tool in the synthesis of a wide array of organic compounds.
Used in Research and Development Laboratories:
Ethyl 3-bromo-2,2-difluoropropionate is primarily used in research settings to explore its potential in creating new compounds with pharmacological and agricultural applications, driving innovation in chemical and life sciences.
Safety Note:
It is crucial to handle Ethyl 3-bromo-2,2-difluoropropionate with care due to its hazardous nature if not properly managed, ensuring safety protocols are strictly followed in laboratory and industrial environments.
Check Digit Verification of cas no
The CAS Registry Mumber 111773-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,7,7 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111773-24:
(8*1)+(7*1)+(6*1)+(5*7)+(4*7)+(3*3)+(2*2)+(1*4)=101
101 % 10 = 1
So 111773-24-1 is a valid CAS Registry Number.
111773-24-1Relevant articles and documents
Easy access to CF2-containing molecules based on the reaction of 2,2,3,3-tetrafluorooxetane with various nucleophiles
Yamada, Shigeyuki,Kato, Masahiro,Komori, Yudai,Konno, Tsutomu,Ishihara, Takashi
experimental part, p. 5493 - 5502 (2011/08/10)
2,2,3,3-Tetrafluorooxetane reacted easily with organolithium reagents to give 1,1,3-trisubstituted 2,2-difluoropropan-1-ols in good to excellent yields. On the other hand, the reaction with Grignard reagent led to 3-bromo-1,1-disubstituted 2,2-difluoropro
Synthese von α-Fluoracrylsaeure und Derivaten
Gassen, K.-R.,Bielefeldt, D.,Marhold, A.,Andres P.
, p. 149 - 162 (2007/10/02)
Three new routes to derivatives of α-fluoracrylic acid, including a laboratory synthesis and a large-scale method, are reported.The processes are (i) addition of elementary fluorine to acrylic esters and subsequent elimination of HF; (ii) addition of difluorocarbene to isopropenyl methyl ether, oxidation via ring opening and dehalogenation; and (iii) "nitrofluorination" of 2,3-dichloropropene, hydrolysis and dechlorination.
N-Aryl 3-Halogenated Azetidin-2-ones and Benzocarbacephems, Inhibitors of β-Lactamases
Joyeau, Roger,Molines, Huguette,Labia, Roger,Wakselman, Michel
, p. 370 - 374 (2007/10/02)
N-(3-Carboxy-6-methylphenyl)-3-fluoroazetidin-2-one and a series of related N-aryl-3-halo- and -3,3-dihaloazetidinones 3, in which the halo substituent is a fluorine or a bromine atom, were prepared, by using the Wasserman procedure of cyclization of β-br
