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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-bromo-3,4-dimethyl-

Cc1c(C)ccnc1Br Request for Quotation
Chemical Name: Pyridine, 2-bromo-3,4-dimethyl-
CAS Number: 33204-85-2
Product Number: AG00CIV8(AGN-PC-03G688)
Synonyms:
MDL No:
Molecular Formula: C7H8BrN
Molecular Weight: 186.0491

Identification/Properties

Computed Properties
Molecular Weight:
186.052g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
184.984g/mol
Monoisotopic Mass:
184.984g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
94.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-3,4-dimethylpyridine is a valuable compound widely utilized in chemical synthesis. Its application lies primarily in organic chemistry, where it serves as a versatile building block for the creation of various complex molecules. This compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.In particular, 2-Bromo-3,4-dimethylpyridine is frequently used in the production of heterocyclic compounds, which are essential in drug discovery and development. Its unique structure and reactivity make it a valuable component in the construction of diverse chemical structures. By serving as a precursor for the introduction of functional groups and stereochemical elements, this compound plays a crucial role in the design and synthesis of bioactive molecules.Furthermore, the incorporation of 2-Bromo-3,4-dimethylpyridine into chemical reactions allows chemists to access a range of reactions and transformations, enabling the preparation of target compounds with high efficiency and selectivity. The versatility of this building block makes it an indispensable tool for chemists working in the field of organic synthesis, enabling the construction of complex molecular architectures with precision and control.