15862-31-4 Usage
Description
2-Amino-3-bromo-5-nitropyridine is an organic compound characterized by its beige to orange-brown powder form. It is a derivative of pyridine, a heterocyclic compound with a nitrogen atom in the ring structure. The presence of an amino group at the 2nd position, a bromine atom at the 3rd position, and a nitro group at the 5th position gives this compound unique chemical properties and reactivity, making it a valuable intermediate in organic synthesis.
Uses
Used in Organic Synthesis:
2-Amino-3-bromo-5-nitropyridine is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows for further functionalization and modification, which can be utilized in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of the amino, bromine, and nitro groups provides multiple points for chemical reactions, enabling the synthesis of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Amino-3-bromo-5-nitropyridine is used as a building block for the synthesis of novel drug candidates. Its versatile chemical properties allow for the development of compounds with potential therapeutic applications, such as new antibiotics, antivirals, or anticancer agents. The compound's reactivity can be exploited to create molecules with specific biological activities, targeting various diseases and conditions.
Used in Agrochemical Industry:
2-Amino-3-bromo-5-nitropyridine also finds application in the agrochemical industry, where it is used as a starting material for the synthesis of new pesticides, herbicides, and insecticides. Its unique structure can be tailored to create compounds with improved efficacy, selectivity, and environmental compatibility, addressing the growing demand for sustainable and effective crop protection solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 15862-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15862-31:
(7*1)+(6*5)+(5*8)+(4*6)+(3*2)+(2*3)+(1*1)=114
114 % 10 = 4
So 15862-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrN3O2/c6-4-1-3(9(10)11)2-8-5(4)7/h1-2H,(H2,7,8)/p+1
15862-31-4Relevant articles and documents
Effect of the 3-halo substitution of the 2′-deoxy aminopyridinyl-pseudocytidine derivatives on the selectivity and stability of antiparallel triplex DNA with a CG inversion site
Wang, Lei,Taniguchi, Yosuke,Okamura, Hidenori,Sasaki, Shigeki
, p. 3853 - 3860 (2017/06/13)
Triplex formation against a target duplex DNA has the potential to become a tool for the genome research. However, there is an intrinsic restriction on the duplex DNA sequences capable of forming the triplex DNA. Recently, we demonstrated the selective fo
