83016-63-1 Usage
Uses
Used in Organic Synthesis:
3,5-dibromo-4-nitrosobenzenesulfonate is utilized as a reagent in organic synthesis, particularly for the preparation of pharmaceuticals and agrochemicals. Its unique structure allows for versatile reactions and the formation of a variety of complex organic molecules.
Used in Biochemical and Biotechnology Applications:
In the modification of proteins and peptides, 3,5-dibromo-4-nitrosobenzenesulfonate serves as a reagent that can alter the properties of these biomolecules, enabling their use in various biochemical and biotechnological applications.
Used in Fluorescent Probe Development:
3,5-dibromo-4-nitrosobenzenesulfonate has been studied for its potential as a fluorescent probe, which can be employed for detecting certain biological molecules. Its fluorescent properties make it a candidate for use in assays and imaging techniques in biological research.
Used in Pharmaceutical Industry:
3,5-dibromo-4-nitrosobenzenesulfonate is used as a key intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-dibromo-4-nitrosobenzenesulfonate is employed in the synthesis of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 83016-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83016-63:
(7*8)+(6*3)+(5*0)+(4*1)+(3*6)+(2*6)+(1*3)=111
111 % 10 = 1
So 83016-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Br2NO4S/c7-4-1-3(14(11,12)13)2-5(8)6(4)9-10/h1-2H,(H,11,12,13)
83016-63-1Relevant academic research and scientific papers
Electron paramagnetic resonance study of the reactions of the spin trap 3,5-dibromo-4-nitrosobenzenesulfonate
Smith, Peter,Robertson, Jill Suzanne
, p. 1153 - 1158 (2007/10/02)
Using rapid-mixing, continuous-flow TiCl3-based techniques and also by means of static-sample studies involving the thermal decomposition of symmetric aliphatic azo compounds, we have characterized by electron paramagnetic resonance 22 spin adducts of 3,5
Lyoluminescence and spin trapping
Ettinger, Kamil V.,Forrester, Alexander R.,Hunter, Charles H.
, p. 1549 - 1559 (2007/10/02)
The chemical origin of lyoluminescence has been probed using spin trapping techniques.Radicals derived from amino acids and saccharides by γ-irradiation in the solid state have been identified after trapping with aliphatic and aromatic nitroso compounds.M
