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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, 5-iodo-N,N-dimethyl-

Ic1ccc(nc1)N(C)C Request for Quotation
Chemical Name: 2-Pyridinamine, 5-iodo-N,N-dimethyl-
CAS Number: 380381-36-2
Product Number: AG00CIS2(AGN-PC-04375X)
Synonyms:
MDL No:
Molecular Formula: C7H9IN2
Molecular Weight: 248.0642

Identification/Properties

Computed Properties
Molecular Weight:
248.067g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
247.981g/mol
Monoisotopic Mass:
247.981g/mol
Topological Polar Surface Area:
16.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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


5-Iodo-N,N-dimethylpyridin-2-amine is a versatile chemical compound commonly used in chemical synthesis applications. It is widely employed as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.One of the key applications of 5-Iodo-N,N-dimethylpyridin-2-amine in chemical synthesis is its role as a precursor in the preparation of heterocyclic compounds. This compound serves as a valuable starting material for the synthesis of diverse heterocycles, including pyridine derivatives, indole derivatives, and other nitrogen-containing ring structures. By participating in a variety of organic reactions such as substitution, cyclization, and coupling reactions, 5-Iodo-N,N-dimethylpyridin-2-amine enables the efficient construction of complex molecular frameworks with potential biological activities.Furthermore, 5-Iodo-N,N-dimethylpyridin-2-amine plays a significant role in the development of novel drug candidates and bioactive molecules. Its incorporation into the molecular structure of target compounds can impart desirable properties such as improved pharmacokinetic profiles, enhanced binding affinity to biological targets, and increased metabolic stability. Through strategic functionalization and derivatization of the amine moiety and the iodine substituent, chemists can access a diverse library of analogs and derivatives for structure-activity relationship studies and lead optimization in drug discovery projects.In summary, 5-Iodo-N,N-dimethylpyridin-2-amine is a valuable tool in the hands of synthetic chemists for the efficient and strategic construction of complex molecules with potential applications in pharmaceuticals, agrochemicals, and other areas of chemical research and development.