16420-30-7 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-3,5-DINITROPYRIDINE is used as a building block for the synthesis of various pharmaceutical compounds. Its reactivity allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-3,5-DINITROPYRIDINE is employed as a precursor in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Industry:
2-BROMO-3,5-DINITROPYRIDINE is utilized as a key intermediate in the production of dyes, enabling the creation of a wide range of colorants for various applications.
Used in Material Science:
Due to its reactive nature, 2-BROMO-3,5-DINITROPYRIDINE is used in the development of new materials, where its unique properties can be harnessed to create innovative products with specific characteristics.
Used in Specialty Chemicals Production:
As an intermediate in the production of specialty chemicals, 2-BROMO-3,5-DINITROPYRIDINE plays a vital role in the synthesis of compounds with unique properties for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16420-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,2 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16420-30:
(7*1)+(6*6)+(5*4)+(4*2)+(3*0)+(2*3)+(1*0)=77
77 % 10 = 7
So 16420-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H2BrN3O4/c6-5-4(9(12)13)1-3(2-7-5)8(10)11/h1-2H
16420-30-7Relevant academic research and scientific papers
Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate
Molander, Gary A.,Cavalcanti, Livia N.
experimental part, p. 4402 - 4413 (2012/06/18)
Organotrifluoroborates have emerged as an alternative to toxic and air- and moisture-sensitive organometallic species for the synthesis of functionalized aryl and heteroaryl compounds. It has been shown that the trifluoroborate moiety can be easily converted into a variety of different substituents in a late synthetic stage. In this paper, we disclose a mild, selective, and convenient method for the ipso-nitrosation of organotrifluoroborates using nitrosonium tetrafluoroborate (NOBF4). Aryl- and heteroaryltrifluoroborates were converted into the corresponding nitroso products in good to excellent yields. This method proved to be tolerant of a broad range of functional groups.
