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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)-

4-(bromomethyl)-2-methylpyridine hydrobromide

BrCc1ccnc(c1)C.Br Request for Quotation
Chemical Name: 4-(bromomethyl)-2-methylpyridine hydrobromide
CAS Number: 1245640-51-0
Product Number: AG01ELSG(AG01ELSG)
Synonyms:
MDL No:
Molecular Formula: C7H9Br2N
Molecular Weight: 266.9611

Identification/Properties

Computed Properties
Molecular Weight:
266.964g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
266.908g/mol
Monoisotopic Mass:
264.91g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
85
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Bromomethyl)-2-methylpyridine hydrobromide is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique structure allows for precise functionalization and modification, making it a valuable tool in synthetic chemistry. This compound is commonly employed in the synthesis of complex organic molecules due to its ability to participate in a variety of important reactions, such as nucleophilic substitution, condensation, and cyclization. Additionally, the presence of both a bromomethyl and a methyl group provides opportunities for selective transformations, enabling the creation of diverse molecular scaffolds. Overall, 4-(Bromomethyl)-2-methylpyridine hydrobromide plays a crucial role in the development of novel compounds and the advancement of synthetic methodologies in the field of organic chemistry.