886371-20-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals due to its reactivity with nucleophiles and its ability to form covalent bonds with a range of substrates. This property makes it a key component in the development of new drugs and pesticides.
Used in Medicinal Chemistry Research:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a reagent in medicinal chemistry research for the development of novel therapeutic agents. Its unique chemical structure and reactivity contribute to the creation of innovative compounds with potential therapeutic applications.
Used in Organic Synthesis:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is used as a reagent in organic synthesis, particularly for the construction of heterocyclic compounds. Its versatility in forming covalent bonds with different substrates makes it an essential tool in the synthesis of complex organic molecules.
Used in Chemical Research:
6-BROMO-PYRIDINE-3-SULFONYL CHLORIDE is utilized in chemical research to explore its reactivity and potential applications in various chemical reactions. Its unique properties allow researchers to investigate new pathways and mechanisms in chemical synthesis and compound development.
Check Digit Verification of cas no
The CAS Registry Mumber 886371-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 886371-20:
(8*8)+(7*8)+(6*6)+(5*3)+(4*7)+(3*1)+(2*2)+(1*0)=206
206 % 10 = 6
So 886371-20-6 is a valid CAS Registry Number.
886371-20-6Relevant articles and documents
Efficient and scalable synthesis of pyridine sulfonamides
Emura, Takashi,Yoshino, Hitoshi,Tachibana, Kazutaka,Shiraishi, Takuya,Honma, Akie,Mizutani, Akemi,Muraoka, Terushige
experimental part, p. 1117 - 1120 (2011/06/20)
Short-step and scalable transformations from 2,6-dibromopyridine to 6-bromopyridine-2-sulfonamide by means of halogen-metal exchange and subsequent reaction with sulfuryl chloride followed by amidation are established. Application of the method for the synthesis of various pyridine sulfonamides is also described. Georg Thieme Verlag Stuttgart - New York.
BI-ARYL AMINOTETRALINES
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Page/Page column 18, (2010/03/04)
The invention is concerned with the compounds of formula I: and pharmaceutically acceptable salts and esters thereof, wherein R1-R5, A, B, Q, W, and X are defined in the detailed description and claims. In addition, the present invention relates to methods of manufacturing and using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds of formula I are antagonists at the CRTH2 receptor and may be useful in treating diseases and disorders associated with that receptor such as asthma.