26482-54-2 Usage
Uses
Used in Pharmaceutical Industry:
N-Nitro-2-pyridinamine is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, N-Nitro-2-pyridinamine serves as a synthetic intermediate for the creation of various dyes. Its chemical properties contribute to the development of dyes with distinct color characteristics and applications in different industries.
Used in Organic Compounds Production:
N-Nitro-2-pyridinamine is utilized as a synthetic intermediate in the production of other organic compounds. Its versatile chemical structure enables its use in the synthesis of a wide range of organic compounds for various applications.
Safety Precautions:
Due to its potential explosive nature and toxicity, N-Nitro-2-pyridinamine requires careful handling and storage. It should be kept away from heat, shock, and friction to prevent accidental detonation. Additionally, proper personal protective equipment, such as gloves, masks, and eye protection, should be worn when handling this chemical to minimize the risk of ingestion, inhalation, or skin contact.
Check Digit Verification of cas no
The CAS Registry Mumber 26482-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26482-54:
(7*2)+(6*6)+(5*4)+(4*8)+(3*2)+(2*5)+(1*4)=122
122 % 10 = 2
So 26482-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N3O2/c9-8(10)7-5-3-1-2-4-6-5/h1-4H,(H,6,7)(H,9,10)/q+1
26482-54-2Relevant academic research and scientific papers
Substituent Effects on the Isomer Ratios in the Rearrangement of Some 2- and 4-Nitraminopyridines
Deady, Leslie W.,Korytsky, Olga L.,Rowe, Jeffrey E.
, p. 2025 - 2034 (2007/10/02)
The preparation, and rearrangement in 92percent sulfuric acid, of 4-X-2-nitramino- (1), 2-X-4-nitramino- (2), and 6-X-2-nitramino-pyridines (3) is reported (X=H,Me,MeO,Br,Cl,CO2H).The product isomer ratios can be explained by differential electronic stabilization of the appropriate ? complexes for aromatic nitration and steric effects seem relatively unimportant.Deuteration had no effect on the product distribution