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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)-

2-Pyridinamine, N,N-dimethyl-5-nitro-

CN(c1ccc(cn1)[N+](=O)[O-])C Request for Quotation
Chemical Name: 2-Pyridinamine, N,N-dimethyl-5-nitro-
CAS Number: 2554-75-8
Product Number: AG00C45I(AGN-PC-0JLPJE)
Synonyms:
MDL No:
Molecular Formula: C7H9N3O2
Molecular Weight: 167.1653

Identification/Properties

Computed Properties
Molecular Weight:
167.168g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
167.069g/mol
Monoisotopic Mass:
167.069g/mol
Topological Polar Surface Area:
62A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Dimethyl-5-nitropyridin-2-amine is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates. Its nitro group can be selectively reduced to an amino group, allowing for further functionalization and modification of the molecule. Additionally, the dimethyl substituents on the nitrogen atom provide steric protection and enhance the stability of the compound during reactions. Overall, N,N-Dimethyl-5-nitropyridin-2-amine plays a crucial role in the synthesis of complex organic molecules with diverse applications in the pharmaceutical and agrochemical industries.