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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, 2-ethenyl-6-methyl-

C=Cc1cccc(n1)C Request for Quotation
Chemical Name: Pyridine, 2-ethenyl-6-methyl-
CAS Number: 1122-70-9
Product Number: AG007BS6(AGN-PC-0JL9W5)
Synonyms:
MDL No:
Molecular Formula: C8H9N
Molecular Weight: 119.1638

Identification/Properties

Computed Properties
Molecular Weight:
119.167g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
119.073g/mol
Monoisotopic Mass:
119.073g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98.7
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


6-Methyl-2-vinylpyridine, a versatile chemical compound, finds widespread application in chemical synthesis due to its unique reactivity and functional properties. In organic synthesis, it serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its vinyl group allows for facile functional group transformations through classic organic chemistry reactions, such as Heck coupling and radical reactions, enabling the creation of a diverse array of compounds. Additionally, the methyl substituent enhances the compound's stability and influences its reactivity profile in complex multistep reactions.