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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)-

Pyridine, 3-(bromomethyl)-2-methyl-

BrCc1cccnc1C Request for Quotation
Chemical Name: Pyridine, 3-(bromomethyl)-2-methyl-
CAS Number: 76915-53-2
Product Number: AG003I73(AGN-PC-0NJWYU)
Synonyms:
MDL No:
Molecular Formula: C7H8BrN
Molecular Weight: 186.0491

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Chemical Structure


3-(Bromomethyl)-2-methylpyridine is a versatile reagent commonly used in chemical synthesis for the introduction of a bromomethyl group into organic molecules. This compound serves as an important building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Due to its unique structure, 3-(Bromomethyl)-2-methylpyridine plays a crucial role in the synthesis of complex organic compounds, particularly in the formation of carbon-carbon and carbon-nitrogen bonds. Its reactivity allows for the functionalization of aromatic systems, enabling the creation of diverse molecular structures with tailored properties. The application of 3-(Bromomethyl)-2-methylpyridine in chemical synthesis offers chemists a valuable tool for the design and preparation of novel compounds with potential applications across different fields.