76893-48-6 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-Methoxyphenoxy)-3-nitropyridine is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(4-Methoxyphenoxy)-3-nitropyridine is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Dye Industry:
2-(4-Methoxyphenoxy)-3-nitropyridine is employed as a key component in the synthesis of dyes, which are used in various applications such as textiles, inks, and pigments.
Used in Organic Chemistry Research:
As a building block in organic chemistry, 2-(4-Methoxyphenoxy)-3-nitropyridine is used for the creation of more complex molecules, facilitating advancements in chemical research and the development of novel compounds.
Used in Material Development:
2-(4-Methoxyphenoxy)-3-nitropyridine has potential applications in the development of new materials, such as polymers and composites, due to its unique chemical structure and properties.
Used as a Reagent in Chemical Research:
In chemical research, 2-(4-Methoxyphenoxy)-3-nitropyridine serves as a reagent, enabling scientists to conduct experiments and explore new chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 76893-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76893-48:
(7*7)+(6*6)+(5*8)+(4*9)+(3*3)+(2*4)+(1*8)=186
186 % 10 = 6
So 76893-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O4/c1-17-9-4-6-10(7-5-9)18-12-11(14(15)16)3-2-8-13-12/h2-8H,1H3
76893-48-6Relevant academic research and scientific papers
Synthesis of near-infrared fluorescent rhodamines via an SNArH reaction and their biological applications
Wang, Qing,Huang, Kun,Cai, Songtao,Liu, Chang,Jiao, Xiaojie,He, Song,Zhao, Liancheng,Zeng, Xianshun
supporting information, p. 7163 - 7169 (2018/10/24)
Near-infrared (NIR) dyes are of great interest in biomedicine due to diminished interfering absorption and fluorescence from biological samples, reduced scattering, and enhanced tissue penetration depth. In this context, we report the synthesis of rectili
Kinetics of the reaction of 2-chloro-3-nitro- and 2-chloro-5-nitropyridines with aryloxide ions in methanol
El-Bardan, Ali A.
, p. 347 - 353 (2007/10/03)
The kinetics of the reaction of 2-chloro-3-nitropyridine (ortho-like) and 2-chloro-5-nitropyridine (para-like) with a series of aryloxide ions were studied in methanol at different temperatures. Plots of ΔH* versus ΔS* for both reactions gave good straight lines with isokinetic temperatures of 168 and 195°C. Good linear relationships were obtained from the plots of log k2 against σ° values with relatively large negative ρ values indicating the formation of Meisenheimer σ-complex intermediates. Plots of log k2 against pKa values gave good straight lines indicating that the reactions show an appreciable degree of bond formation in the transition state. An addition-elimination mechanism is suggested. Copyright
