885952-16-9 Usage
Uses
Used in Pharmaceutical Industry:
2,3-DIBROMO-6-CHLOROPYRIDINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2,3-DIBROMO-6-CHLOROPYRIDINE is used as a potent bactericide and fungicide for controlling a wide range of microbial pests in agriculture. Its effectiveness in managing plant diseases contributes to increased crop yields and reduced losses.
Used in Organic Synthesis:
2,3-DIBROMO-6-CHLOROPYRIDINE is used as a reagent in the preparation of heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Safety Precautions:
Due to its potential hazards to human health and the environment, it is crucial to follow proper safety precautions when handling and storing 2,3-Dibromo-6-chloropyridine. This includes using appropriate personal protective equipment, ensuring proper ventilation, and adhering to disposal regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 885952-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,9,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885952-16:
(8*8)+(7*8)+(6*5)+(5*9)+(4*5)+(3*2)+(2*1)+(1*6)=229
229 % 10 = 9
So 885952-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Br2ClN/c6-3-1-2-4(8)9-5(3)7/h1-2H
885952-16-9Relevant academic research and scientific papers
Chamas,Marchi,Presson,Aubert,Fort,Ceroni,Mamane
, p. 2715 - 2723 (2015)
With the aim to design fluorescent solids, a series of indeno[1′,2′:4,5]pyrido[2,1-a]isoindol-5-ones with various substituents was prepared. In these π-extended pentacyclic derivatives, the presence of a methyl group in the 7-position was found to have a critical influence on the fluorescence properties in the solid state. Crystal packing of the non-substituted derivatives shows strong π-π interactions causing quenching of the fluorescence. In contrast, by introducing a methyl substituent in the 7-position we obtained compounds with fluorescence quantum yield up to 32% in the solid state.
