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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Pyridinamine, N-methyl-3-nitro-

CNc1ccncc1[N+](=O)[O-] Request for Quotation
Chemical Name: 4-Pyridinamine, N-methyl-3-nitro-
CAS Number: 1633-41-6
Product Number: AG001U0H(AGN-PC-0JSTVE)
Synonyms:
MDL No:
Molecular Formula: C6H7N3O2
Molecular Weight: 153.1387

Identification/Properties

Properties
MP:
159-162°C
BP:
299.5±25.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
153.141g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
153.054g/mol
Monoisotopic Mass:
153.054g/mol
Topological Polar Surface Area:
70.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
145
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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Methyl-3-nitropyridin-4-amine is a versatile compound utilized in chemical synthesis for its unique properties and reactivity. With a methyl group attached to the nitrogen atom and a nitro group on the pyridine ring, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals.In organic synthesis, N-Methyl-3-nitropyridin-4-amine can act as a nucleophile, allowing for the introduction of the nitrogen-containing pyridine moiety into different molecular frameworks. It can also participate in various coupling reactions to form more complex molecules with tailored properties. Additionally, the nitro group can be utilized as a directing group in metal-catalyzed reactions, enabling selective functionalization at specific positions on the pyridine ring.Furthermore, the presence of a methyl group enhances the compound's solubility and stability, making it easier to handle and manipulate in different synthetic processes. Its compatibility with a wide range of reaction conditions and reagents makes N-Methyl-3-nitropyridin-4-amine a valuable intermediate in the synthesis of intricate organic molecules with diverse applications in the chemical industry.