118807-77-5 Usage
Uses
Used in Pharmaceutical Industry:
[(3-nitropyridin-2-yl)amino]acetic acid is used as a building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(3-nitropyridin-2-yl)amino]acetic acid is utilized as a starting material for the development of novel agrochemicals, such as pesticides and herbicides, that can help improve agricultural productivity and crop protection.
Used in Materials Science:
[(3-nitropyridin-2-yl)amino]acetic acid's properties make it a candidate for use in the field of materials science, where it can be employed in the development of new materials with specific characteristics, such as improved conductivity or enhanced stability.
Used as a Fluorescent Probe in Bioimaging:
Due to its fluorescent properties, [(3-nitropyridin-2-yl)amino]acetic acid can be used as a probe in bioimaging applications. This allows researchers to visualize and study biological processes at the molecular level, contributing to a better understanding of various biological phenomena and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 118807-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,0 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 118807-77:
(8*1)+(7*1)+(6*8)+(5*8)+(4*0)+(3*7)+(2*7)+(1*7)=145
145 % 10 = 5
So 118807-77-5 is a valid CAS Registry Number.
118807-77-5Relevant academic research and scientific papers
SYNTHESES OF FUNCTIONALIZED N-(2-PYRIDYL)-α-AMINO ACIDS AND ESTERS BY RING OPENING OF IMIDAZOPYRIDINE
Doise, Muriel,Blondeau, Dominique,Sliwa, Henri
, p. 2079 - 2093 (2007/10/02)
This report is devoted to the ring opening of the imidazole nucleus of functionalized imidazopyridines, by methanol in strong acid medium (HClO4) leading to esters of N-(2-pyridyl)-α-amino acids in which the heterocyclic moiety bears a functional g
o-Nitroaniline Derivatives. Part 9. Benzimidazole N-Oxides Unsubstituted at N-1 and C-2
Harvey, Ian W.,McFarlane, Michael D.,Moody, David J.,Smith, David M.
, p. 681 - 690 (2007/10/02)
Since previous routes to the title compounds (1) have proved unsatisfactory as general methods, a simple new synthesis has been devised.N-Cyanomethyl-o-nitroanilines (5) are cyclised in basic media, giving 2-cyanobenzimidazole N-oxides (12) in good yield.Hydrolysis of these products with hydrochloric acid gives, directly, the title compounds as their hydrochloride salts (13), which may be isolated and purified, and which give the free N-oxides (1) by treatment with aqueous ammonia followed by evaporation. o-Nitrophenylglycine esters (4) may satisfactorily replace the nitriles (5) in certain cases.A modification of this kind in the related nitropyridylglycine series leads to 3H-imidazolpyridine 1-oxide (20).
