33245-29-3 Usage
Uses
Used in Pharmaceutical Industry:
5-Bromo-N-nitropyridin-2-amine is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
5-broMo-N-nitropyridin-2-aMine also serves as an intermediate in the production of agrochemicals, playing a crucial role in the creation of pesticides and other agricultural products that are essential for maintaining crop health and productivity.
Used in Dye Manufacturing:
5-Bromo-N-nitropyridin-2-amine is employed in the manufacture of dyes, where its chemical properties are harnessed to produce a range of colors and shades for various applications, including textiles, plastics, and printing inks.
Used in Organic Compound Synthesis:
Due to its ability to participate in numerous chemical reactions, 5-Bromo-N-nitropyridin-2-amine is a versatile building block in the synthesis of organic compounds. This makes it a valuable resource for researchers and chemical manufacturers looking to create new and innovative products across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 33245-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33245-29:
(7*3)+(6*3)+(5*2)+(4*4)+(3*5)+(2*2)+(1*9)=93
93 % 10 = 3
So 33245-29-3 is a valid CAS Registry Number.
33245-29-3Relevant academic research and scientific papers
Syntheses with Aromatic Nitramines. IX. Halogenation of 2- and 4-Nitraminopyridines
Brzozka, L.,Baran, W.,Kraus, W.,Tomasik, P.
, p. 605 - 611 (2007/10/02)
Isomeric 2- and 4-nitraminopyridines (free acids and anions) were subjected to halogenation (iodination, bromination and chlorination).The iodination of nitraminopyridine anions failed, and the bromination and chlorination led selectively to 5-monohalogenated products independently of whether free acids or anions of nitraminopyridines were reacted.Key words: nitraminopyridines, halogenation
