54079-68-4 Usage
Uses
Used in Pharmaceutical Production:
4-Chloro-3-nitropyridine hydrochloride is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-Chloro-3-nitropyridine hydrochloride serves as a building block for the creation of pesticides and other agricultural chemicals. Its reactivity and functional groups make it suitable for the production of effective and targeted agrochemicals.
Used in Dye Manufacturing:
4-Chloro-3-nitropyridine hydrochloride is utilized in the manufacturing of dyes due to its ability to impart color. Its chemical properties allow it to be integrated into dye molecules, enhancing the colorfastness and performance of the dyes in various applications.
Used in Organic Synthesis:
As a versatile intermediate, 4-Chloro-3-nitropyridine hydrochloride is employed in organic synthesis for a wide range of chemical reactions. Its presence in various synthetic pathways enables the production of diverse chemical compounds, expanding the scope of organic chemistry.
Used in Laboratory Research:
4-Chloro-3-nitropyridine hydrochloride is used as a research compound in laboratories to study its properties and potential applications. Its water solubility and reactivity make it an ideal candidate for exploring new chemical reactions and understanding its behavior in different chemical environments.
Check Digit Verification of cas no
The CAS Registry Mumber 54079-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,7 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54079-68:
(7*5)+(6*4)+(5*0)+(4*7)+(3*9)+(2*6)+(1*8)=134
134 % 10 = 4
So 54079-68-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClN2O2.ClH/c6-4-1-2-7-3-5(4)8(9)10;/h1-3H;1H
54079-68-4Relevant articles and documents
Antiviral azaindole derivatives
-
, (2008/06/13)
The present invention is directed to a series of chemical entities that express HIV-1 inhibitory activities.
Pyrolysis of Aryl Azides. VI Identification of Neighbouring Group Effects in Pyrolysis of Azidopyridines and Azidoquinolines
Dyall, Leonard K.,Wah, Wong Ming
, p. 1045 - 1059 (2007/10/02)
Although there are literature reports of anomalous behaviour on pyrolysis of ortho-nitroazidopyridines and ortho-nitroazidoquinolines, we find that these compounds cyclize to the expected furazan 1-oxides in near-quantitative yields, and with a high degree of neighbouring group participation by the nitro group.Kinetic studies in decalin solution reveal the following rate enhancements by the ortho-nitro group: 3-azido-2-nitropyridine, 466 at least; 4-azido-3-nitropyridine, 5400; 4-azido-3,5-dinitropyridine, 640; 4-azido-3-nitroquinoline, 82.4; 5-azido-6-nitroquinoline,27.6; 2-nitro-1-azidonaphthalene, 12.7.The unstable furazan oxide, oxadiazolopyridine 1-oxide, has now been characterized. Oxadiazolopyridine 1-oxide decomposed in decalin at 145 deg to give products indicative of a nitrene intermediate.