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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)-

7-Quinolinamine, 4-methyl-

Nc1ccc2c(c1)nccc2C Request for Quotation
Chemical Name: 7-Quinolinamine, 4-methyl-
CAS Number: 114058-79-6
Product Number: AG000AF7(AGN-PC-0JS0SZ)
Synonyms:
MDL No:
Molecular Formula: C10H10N2
Molecular Weight: 158.1998

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Chemical Structure


With its versatile applications in chemical synthesis, 4-Methylquinolin-7-amine serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound, known for its unique structure and reactivity, plays a crucial role in the development of novel compounds and materials. Its compatibility with a wide range of reaction conditions makes it a valuable tool for organic chemists seeking to design and synthesize complex molecules efficiently. Due to its functional groups and strategic positions, 4-Methylquinolin-7-amine enables the introduction of diverse substituents and structural modifications, allowing for the synthesis of tailored molecules with specific properties and functionalities. In both academic research and industrial settings, this compound is employed in the creation of bioactive compounds, fluorescent dyes, and advanced materials, demonstrating its significance in advancing the field of chemical synthesis.