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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-(bromomethyl)-4,6-dimethyl-

BrCc1cc(C)cc(n1)C Request for Quotation
Chemical Name: Pyridine, 2-(bromomethyl)-4,6-dimethyl-
CAS Number: 79313-01-2
Product Number: AG00G47A(AGN-PC-03NA0L)
Synonyms:
MDL No:
Molecular Formula: C8H10BrN
Molecular Weight: 200.0757

Identification/Properties

Computed Properties
Molecular Weight:
200.079g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
199g/mol
Monoisotopic Mass:
199g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Bromomethyl)-4,6-dimethylpyridine is a versatile compound widely used in chemical synthesis as a key building block for various organic reactions. Due to its unique molecular structure, this compound exhibits strong reactivity and selectivity, making it highly valuable in the synthesis of complex organic molecules. One of the primary applications of 2-(Bromomethyl)-4,6-dimethylpyridine is in the formation of carbon-carbon (C-C) and carbon-heteroatom bonds through nucleophilic substitution and cross-coupling reactions. Additionally, this compound is employed as a precursor for the synthesis of pharmaceuticals, agrochemicals, dyes, and other fine chemicals. Its ability to undergo selective functionalization at the bromomethyl and methyl positions enables chemists to access a wide range of derivatives with tailored properties and functionalities. In summary, 2-(Bromomethyl)-4,6-dimethylpyridine plays a crucial role in the construction of complex organic frameworks and the development of novel chemical entities in the field of synthetic chemistry.