104222-46-0 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 3-bromo-2,4,5-trifluorobenzoylacetate is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 3-bromo-2,4,5-trifluorobenzoylacetate is employed as an intermediate for the production of agrochemicals. Its involvement in the synthesis of these chemicals aids in the development of effective solutions for pest control and crop protection, thereby supporting agricultural productivity.
Used in Organic Synthesis:
Ethyl 3-bromo-2,4,5-trifluorobenzoylacetate is used as a reagent in organic synthesis, particularly for the synthesis of heterocyclic compounds. These compounds are vital in various applications, including the development of pharmaceuticals, agrochemicals, and other specialty chemicals, showcasing the versatility of this intermediate in chemical reactions.
Used in Fine Chemicals Production:
Ethyl 3-bromo-2,4,5-trifluorobenzoylacetate also plays a role in the production of fine chemicals, which are high-purity chemicals used in various industries such as pharmaceuticals, fragrances, and flavors. Ethyl 3-bromo-2,4,5-trifluorobenzoylacetate's contribution to the synthesis of these fine chemicals highlights its importance in creating high-quality products for diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 104222-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,2 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104222-46:
(8*1)+(7*0)+(6*4)+(5*2)+(4*2)+(3*2)+(2*4)+(1*6)=70
70 % 10 = 0
So 104222-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H8BrF3O3/c1-2-18-8(17)4-7(16)5-3-6(13)11(15)9(12)10(5)14/h3H,2,4H2,1H3
104222-46-0Relevant academic research and scientific papers
The synthesis of 3-bromo-2,4,5-trifluorobenzoic acid and its conversion to 8-bromoquinolonecarboxylic acids
Renau, Thomas E.,Sanchez, Joseph P.,Domagala, John M.
, p. 1407 - 1411 (2007/10/03)
A series of 8-bromo-4-oxo-3-quinolinecarboxylic acids was prepared via the borate ester, 8. The key intermediate in the synthesis of the final products 10a-10d was 3-bromo-2,4,5-trifluorobenzoic acid (3), conveniently prepared in two steps from the known oxazoline, 1. The preparation of 10a-10d is a significant improvement of the literature procedure currently available for the synthesis of these compounds.
Quinolonecarboxylic acid derivatives
-
, (2008/06/13)
Quinolonecarboxylic acid derivatives of the following formula, STR1 wherein R1, R2, R3 and R4 are each independently hydrogen atom or lower alkyl group; the hydrates or the pharmaceutically acceptable acid addit
