13505-07-2 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Methoxy-4-nitropyridine is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 3-Methoxy-4-nitropyridine serves as a key component in the production of certain pesticides and herbicides. Its chemical properties enable the creation of effective compounds for controlling pests and weeds in agricultural settings.
Used in Material Science Applications:
3-Methoxy-4-nitropyridine also finds use in material science, where it can be incorporated into the development of new materials with specific properties. Its versatility in chemical reactions allows for the creation of materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13505-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13505-07:
(7*1)+(6*3)+(5*5)+(4*0)+(3*5)+(2*0)+(1*7)=72
72 % 10 = 2
So 13505-07-2 is a valid CAS Registry Number.
13505-07-2Relevant academic research and scientific papers
COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY
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Page/Page column 125, (2022/01/24)
The present invention relates to chemical entities (for example, a pharmaceutically acceptable compound or salt, and / or a hydrate, and / or a co-crystal, and / or a combination of drug of the compound) which inhibit (for example, antagonize) the stimula
Preparation method of cisapride key intermediate
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, (2019/01/06)
The invention provides a preparation method of a cisapride key intermediate. The preparation method includes the steps of adopting 3-pyridine as an initial raw material, 3-methoxypyridine is synthesized through nucleophilic substitution, 4-nitryl-3-methoxypyridine is prepared through a nitration reaction, a 4-nitryl-3-methoxyl-N-(3-(4-fluorophenoxy)propyl) quaternized pyridinium is prepared through quaternization, and the cisapride key intermediate, namely (cis)-N-(3-(4-fluorophenoxy)propyl)-4-amino-3-methoxy piperidine, is prepared through catalytic hydrogenation at last. The preparation method has the advantages of being low in cost, easy to operate and the like.
