71702-00-6 Usage
Uses
Used in Pharmaceutical Industry:
5-Bromo-6-chloronicotinaldehyde is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs.
Used in Agrochemical Industry:
5-Bromo-6-chloronicotinaldehyde is used as an intermediate in the synthesis of agrochemicals for its potential to be part of molecules that can help in the development of pesticides or other agricultural products.
Used in Organic Synthesis:
5-Bromo-6-chloronicotinaldehyde is used as a building block in organic synthesis for its ability to be combined with other compounds to create a wide range of organic molecules, facilitating the creation of new chemical entities.
Used in Chemical Research:
5-Bromo-6-chloronicotinaldehyde is used as a reagent in chemical research for its potential to be involved in various chemical reactions, aiding in the discovery and understanding of new chemical processes and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 71702-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71702-00:
(7*7)+(6*1)+(5*7)+(4*0)+(3*2)+(2*0)+(1*0)=96
96 % 10 = 6
So 71702-00-6 is a valid CAS Registry Number.
71702-00-6Relevant academic research and scientific papers
VIRAL POLYMERASE INHIBITORS
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Page/Page column 94, (2009/04/25)
Compound of Formula I: wherein, R2, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase
Herbicidal pyridine compounds
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, (2008/06/13)
Herbicidal 3- and/or 5-halogenomethyl-pyrid-2-yloxyphenoxy compounds and processes for making and using the same. Intermediates for making these compounds and their preparation are also disclosed. Thus, for example, 2-chloro-5-trichloromethylpyridine is prepared by a liquid phase chlorination of 3-methylpyridine under the influence of ultra violet light.
