122433-50-5 Usage
Uses
Used in Organic Synthesis:
Methyl 2-Methoxy-5-nitronicotinic acid is used as a building block in organic synthesis for the creation of various organic compounds. Its unique structure, including the methoxy and nitro groups, allows for versatile reactions and the formation of a range of chemical products.
Used in Pharmaceutical Research:
In pharmaceutical research, Methyl 2-Methoxy-5-nitronicotinic acid is employed as a key intermediate for the development of new drugs. Its properties make it a valuable component in the synthesis of pharmaceutical compounds, contributing to the discovery and production of novel medications.
Used in Agrochemical Production:
Methyl 2-Methoxy-5-nitronicotinic acid is utilized as an intermediate in the production of agrochemicals. Its role in this industry is crucial for the synthesis of various agrochemicals that are used in agriculture to protect crops and enhance yields.
Used in Pharmaceutical Production:
As an intermediate in pharmaceutical production, Methyl 2-Methoxy-5-nitronicotinic acid plays a significant role in the synthesis of a variety of pharmaceuticals. Its presence in the manufacturing process is essential for the development of new medicines and the improvement of existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 122433-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,3 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122433-50:
(8*1)+(7*2)+(6*2)+(5*4)+(4*3)+(3*3)+(2*5)+(1*0)=85
85 % 10 = 5
So 122433-50-5 is a valid CAS Registry Number.
122433-50-5Relevant academic research and scientific papers
Spiro hydantoin aldose reductase inhibitors derived from 8-aza-4-chromanones
Sarges,Goldstein,Welch,Swindell,Siegel,Beyer
, p. 1859 - 1865 (2007/10/02)
A series of spiro hydantoins derived from 8-azachromanones (2,3-dihydro-4H-pyrano[2,3-b]pyridin-4-ones) has been prepared and tested for aldose reductase inhibitory activity. The standard Bucherer-Bergs conditions had to be drastically modified to increas
