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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-bromo-6-ethenylpyridine

C=Cc1cccc(n1)Br Request for Quotation
Chemical Name: 2-bromo-6-ethenylpyridine
CAS Number: 931582-13-7
Product Number: AG006I3P(AGN-PC-04ZBZI)
Synonyms:
MDL No:
Molecular Formula: C7H6BrN
Molecular Weight: 184.0332

Identification/Properties

Properties
Form:
Liquid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 2-Bromo-6-vinylpyridine in chemical synthesis is crucial in various organic reactions due to its unique properties. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and fine chemicals. With its vinyl group and bromine substituent, 2-Bromo-6-vinylpyridine enables the introduction of diverse functionalities into organic molecules through cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings. Additionally, this compound can undergo various substitution reactions to yield derivatives with altered chemical and physical properties, making it a versatile tool in the synthesis of complex organic compounds.