864550-41-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Hydroxy-4-bromo-6-nitrotoluene is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicines. Its unique structure allows it to be a key component in the creation of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Hydroxy-4-bromo-6-nitrotoluene serves as an intermediate in the production of agrochemicals, playing a role in the development of pesticides and other agricultural products to enhance crop protection and yield.
Used in Dye and Pigment Production:
This chemical compound is utilized in the production of dyes and pigments, where its properties contribute to the creation of a wide range of colors and hues for various applications, including textiles, plastics, and printing inks.
Used in Organic Compound Preparation:
2-Hydroxy-4-bromo-6-nitrotoluene is used as a building block in the preparation of a variety of organic compounds, showcasing its versatility and importance in organic chemistry for synthesizing complex molecules.
Safety Precautions:
Given that 2-hydroxy-4-bromo-6-nitrotoluene is a flammable and potentially hazardous chemical, it is crucial to handle it with proper safety measures. This includes taking precautions to prevent ignition sources, using appropriate personal protective equipment, and adhering to guidelines for storage and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 864550-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,5,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 864550-41:
(8*8)+(7*6)+(6*4)+(5*5)+(4*5)+(3*0)+(2*4)+(1*1)=184
184 % 10 = 4
So 864550-41-4 is a valid CAS Registry Number.
864550-41-4Relevant academic research and scientific papers
A Concise Total Synthesis of Breitfussin A and B
Pandey, Sunil Kumar,Guttormsen, Yngve,Haug, Bengt Erik,Hedberg, Christian,Bayer, Annette
, p. 122 - 125 (2015/07/28)
(Chemical Equation Presented). The first total synthesis of breitfussin A and B is described. The approach features two palladium-catalyzed cross-couplings installing the indole and pyrrole onto the oxazole core and selective lithiation/iodination of a common indole-oxazole fragment providing 2,4-diiodinated or 2-iodinated oxazoles as potential precursors for breitfussin A and B, respectively. An unexpected acid promoted deiodination was utilized in the synthesis of breitfussin B. Comparison of the synthetic material with previously reported spectral data of isolated breitfussin A and B verified the structure of the breitfussin framework.
Pyranouidole Derivatives and the Use Thereof for the Treatment of Hepatitis C Virus Infection or Disease
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Page/Page column 18-19, (2010/11/28)
The invention is directed to novel pyranoindole derivatives and analogs as well as compositions containing the same and to the use thereof for the treatment, prevention or inhibition of viral infections and associated diseases caused by the Hepatitis C vi
