799246-56-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Bromo-2-vinylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-2-vinylpyridine is utilized as an intermediate for the production of agrochemicals. Its role in creating effective pesticides and other agricultural chemicals helps to improve crop protection and yield.
Used in Organic Compounds Production:
3-Bromo-2-vinylpyridine is used as a building block in the synthesis of a wide range of organic compounds. Its versatility in chemical reactions enables the creation of diverse molecules with various applications in different industries.
Used in Polymer Production:
3-Bromo-2-vinylpyridine is used in the polymerization process to form various polymers. These polymers have potential uses in multiple industries, including plastics, coatings, and adhesives, due to their unique properties derived from the 3-Bromo-2-vinylpyridine monomer.
Check Digit Verification of cas no
The CAS Registry Mumber 799246-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 799246-56:
(8*7)+(7*9)+(6*9)+(5*2)+(4*4)+(3*6)+(2*5)+(1*6)=233
233 % 10 = 3
So 799246-56-3 is a valid CAS Registry Number.
799246-56-3Relevant articles and documents
Enantioselective Construction of Spiro Quaternary Carbon Stereocenters via Pd-Catalyzed Intramolecular α-Arylation
Wu, Ting,Kang, Xuehua,Bai, Heng,Xiong, Wenrui,Xu, Guangqing,Tang, Wenjun,Tang, Wenjun
supporting information, p. 4602 - 4607 (2020/06/29)
We herein report the development of a sterically hindered and electron-rich P-chiral monophosphorus biaryl ligand that has enabled a general and efficient enantioselective intramolecular α-arylation, providing access to a wide series of [4.4], [4.5], and [4.6]-spirocycles with chiral benzylic quaternary carbons in high yields with good to excellent enantioselectivities. A pronounced water effect on enantioselectivity is observed.