3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-nitroso-, methyl ester


Chemical Name: 3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-nitroso-, methyl ester
CAS Number: 55557-02-3
Product Number: AG00DFG3(AGN-PC-0JL4U8)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O3
Molecular Weight: 170.1659

Identification/Properties


Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
170.168g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
170.069g/mol
Monoisotopic Mass:
170.069g/mol
Topological Polar Surface Area:
59A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
225
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



Nitrosoguvacoline is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. As a source of nitric oxide, Nitrosoguvacoline plays a crucial role in various reactions due to its ability to donate nitric oxide under mild conditions. This compound is particularly valued for its role as a nitrosating agent, where it can introduce nitroso functional groups into various organic molecules, leading to the synthesis of a wide range of important compounds.In organic synthesis, Nitrosoguvacoline is commonly used to nitrosate amines, thiols, and other nucleophiles, leading to the formation of nitroso derivatives. These nitroso compounds have applications in the pharmaceutical industry, as they can act as precursors for the synthesis of pharmaceuticals and agrochemicals. Additionally, nitrosated products can also serve as valuable intermediates in the synthesis of natural products and complex organic molecules.Furthermore, Nitrosoguvacoline can also participate in reactions such as the Griess diazotization reaction, where it reacts with primary aromatic amines to form diazo compounds. These diazo compounds have diverse applications in the synthesis of azo dyes, pharmaceuticals, and other organic compounds.Overall, the versatile nature of Nitrosoguvacoline in chemical synthesis makes it an indispensable tool for organic chemists looking to access a wide variety of functionalized organic molecules with important applications in various industries.