5832-44-0 Usage
Uses
Used in Pharmaceutical and Chemical Synthesis:
4-Methyl-3-nitropyridine is used as a starting material for the synthesis of various organic compounds, particularly in the pharmaceutical industry. Its unique structure allows for the creation of a wide range of derivatives with potential applications in drug development.
Used in Ethyl 6-Azaindole-2-Carboxylate Synthesis:
4-Methyl-3-nitropyridine serves as a key intermediate in the synthesis of ethyl 6-azaindole-2-carboxylate, a compound that may have potential applications in the development of pharmaceuticals and other organic compounds.
Used in 3-Substituted Azaindoles Synthesis:
4-Methyl-3-nitropyridine is also utilized in the synthesis of 3-substituted azaindoles, which are a class of heterocyclic compounds with potential applications in medicinal chemistry and as building blocks for the development of new drugs.
Used in Research Chemistry:
4-Methyl-3-nitropyridine is a useful research chemical, employed by scientists and researchers to study its properties, reactivity, and potential applications in various fields, including material science and pharmaceuticals. Its unique structure and reactivity make it an interesting subject for further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 5832-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5832-44:
(6*5)+(5*8)+(4*3)+(3*2)+(2*4)+(1*4)=100
100 % 10 = 0
So 5832-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-5-2-3-7-4-6(5)8(9)10/h2-4H,1H3
5832-44-0Relevant academic research and scientific papers
Selective ortho methylation of nitroheteroaryls by vicarious nucleophilic substitution
Achmatowicz, Michal,Thiel, Oliver R.,Gorins, Gilles,Goldstein, Corinne,Affouard, Caroline,Jensen, Randy,Larsen, Robert D.
, p. 6793 - 6799 (2008/12/22)
(Chemical Equation Presented) An efficient and scalable three-step one-pot approach to 6-methyl-5-nitroisoquinoline (1) from inexpensive 5-nitroisoquinoline, utilizing the vicarious nucleophilic substitution (VNS) as a key step, is described. The optimized reaction conditions can be applied to a limited number of other aromatic and heteroaromatic nitro compounds. Attempts to understand the observed selectivity in the VNS step led to the discovery of two new reaction pathways under VNS conditions, one leading to an isoxazole and the other resulting in the formal cyclopropanation of an aromatic nitro compound.
