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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, 2,3-dimethyl-

Cc1c(N)ccnc1C Request for Quotation
Chemical Name: 4-Pyridinamine, 2,3-dimethyl-
CAS Number: 122475-57-4
Product Number: AG0017B0(AGN-PC-0LYN15)
Synonyms:
MDL No: MFCD00030819
Molecular Formula: C7H10N2
Molecular Weight: 122.1677

Identification/Properties

Properties
BP:
269°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
122.171g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
122.084g/mol
Monoisotopic Mass:
122.084g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
92.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-2,3-dimethylpyridine, a versatile chemical compound, plays a crucial role in chemical synthesis processes. Its application in organic chemistry particularly shines through its ability to act as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. The presence of an amino group and a methyl substituent on the pyridine ring make it an ideal candidate for use in heterocyclic chemistry, enabling the synthesis of complex molecules with diverse functionalities. Specifically, 4-Amino-2,3-dimethylpyridine can be employed in the formation of fused ring systems, substitution reactions, and as a catalyst in various transformations. Its unique structural properties and reactivity make it a valuable component in the toolbox of synthetic chemists striving to develop innovative compounds for a range of industrial applications.