205683-34-7 Usage
Uses
Used in Pharmaceutical Industry:
2,4-DIBROMO-6-FLUOROBENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2,4-DIBROMO-6-FLUOROBENZALDEHYDE serves as an essential building block in the creation of compounds that are used to protect crops from pests and diseases, enhancing agricultural productivity.
Used in Dye Manufacturing:
2,4-DIBROMO-6-FLUOROBENZALDEHYDE is utilized as an intermediate in the production of dyes, where its unique molecular structure contributes to the color properties and stability of the final dye products.
Used in Organic Chemistry Research:
As a chemical intermediate, 2,4-DIBROMO-6-FLUOROBENZALDEHYDE is also used in organic chemistry research for exploring new reactions and developing innovative synthetic pathways, further expanding the scope of chemical science.
It is crucial to handle 2,4-DIBROMO-6-FLUOROBENZALDEHYDE with care due to its potential hazards if mismanaged, ensuring safety in its applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 205683-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,6,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 205683-34:
(8*2)+(7*0)+(6*5)+(5*6)+(4*8)+(3*3)+(2*3)+(1*4)=127
127 % 10 = 7
So 205683-34-7 is a valid CAS Registry Number.
205683-34-7Relevant academic research and scientific papers
Synthesis and Transformations of Functionalized Benzosiloxaboroles
Czub, Maja,Durka, Krzysztof,Luliński, Sergiusz,?osiewicz, Justyna,Serwatowski, Janusz,Urban, Mateusz,Wo?niak, Krzysztof
, p. 818 - 826 (2017/02/15)
The synthesis and characterization of a series of fluorinated benzosiloxaboroles bearing synthetically useful formyl and cyano groups is reported. These compounds have been obtained by multistep syntheses starting with simple halogenated benzenes. The general synthetic protocol was based on the generation of ortho-boronated aryldimethylsilanes which undergo dehydrogenative cyclization upon hydrolytic workup due to activation of the Si–H bond by the adjacent boronic group. In some cases the synergy of adjacent boron- and silicon-based functionalities resulted in an unexpected hydrosilylation of the CHO group under mild aqueous conditions. The reduction of a benzosiloxaborole derivative bearing the formyl group at the ortho position with respect to the boron atom resulted in a structural transformation reflecting the higher stability of the carboxaborole heterocycle with respect to its silicon counterpart. Thus, a unique heterocyclic system featuring a central 10-membered ring comprising two borasiloxane linkages was isolated.
Aralkyl and aralkylidene heterocyclic lactams and imides
-
, (2008/06/13)
The present invention relates to compounds of the formula I wherein R1, R2, R3, X, Y and the dashed line are as defined in the specification, to intermediates for their preparation, to pharmaceutical compositions containin
