18700-11-3 Usage
Uses
Used in Pharmaceutical Industry:
2,6-DICHLORO-3-PHENYLPYRIDINE is used as a building block for the synthesis of pharmaceutical compounds and agrochemicals. Its unique structure and reactivity contribute to the development of new drugs and chemical entities that can address various health concerns.
Used in Organic Synthesis:
2,6-DICHLORO-3-PHENYLPYRIDINE is used as a valuable intermediate in organic synthesis. Its presence in the synthesis process allows for the creation of a wide range of chemical products, including those with potential applications in medicine, agriculture, and other industries.
Used in Anti-Tuberculosis Drug Research:
2,6-DICHLORO-3-PHENYLPYRIDINE is being studied for its potential use as an anti-tuberculosis drug. Its biological activities and pharmacological properties are under investigation to determine its efficacy and safety in treating tuberculosis.
Used in Biological Activity Studies:
2,6-DICHLORO-3-PHENYLPYRIDINE is used in research to explore its biological activities. Understanding its interactions with biological systems can lead to the discovery of new therapeutic agents or insights into disease mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 18700-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18700-11:
(7*1)+(6*8)+(5*7)+(4*0)+(3*0)+(2*1)+(1*1)=93
93 % 10 = 3
So 18700-11-3 is a valid CAS Registry Number.
18700-11-3Relevant academic research and scientific papers
Diels-Alder reactions of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones with alkynes: Synthesis of 3,5-disubstituted 2,6-dichloropyridines
Meerpoel,Deroover,Van Aken,Lux,Hoornaert
, p. 765 - 768 (2007/10/02)
The Diels-Alder reactiion of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones 1 with different types of acetylenic compounds 2 is shown to be a versatile method for the generation of variously substituted 2,6-dichloropyridines. In most cases a high degree of reg
GENERATION OF SPECIFICALLY SUBSTITUTED PYRIDINES AND PYRIDONES FROM 2(1H) PYRAZINONES AND ACETYLENES: A FMO DESCRIPTION
Tutonda, M.,Vanderzande, D.,Hendrickx, M.,Hoornaert, G.
, p. 5715 - 5732 (2007/10/02)
The title compounds were obtained from reaction of variously substituted 2(1H)pyrazinones with acetylenic derivatives.Experimental evidence points out to a two step mechanism: a Diels Alder cycloaddition followed by immediate decomposition of the adducts
DIELS-ALDER REACTIONS OF THE HETERODIENE SYSTEM IN 2(1H)-PYRAZINONES
Tutonda, M.,Vanderzande, D.,Vekemans, J.,Toppet, S.,Hoornaert, G.
, p. 2509 - 2512 (2007/10/02)
Variously substituted 2(1H)-pyrazinones react with acetylenic derivatives to give specifically substituted pyridones or pyridines.The observed selectivity can be explained in terms of HO-LU interactions for the reagents and two competitive retro Diels-Ald
