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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-3-(bromomethyl)-6-methylpyridine

Cc1ccc(c(n1)Br)CBr Request for Quotation
Chemical Name: 2-Bromo-3-(bromomethyl)-6-methylpyridine
CAS Number: 944707-38-4
Product Number: AG00II6T(AGN-PC-0WAIAI)
Synonyms:
MDL No:
Molecular Formula: C7H7Br2N
Molecular Weight: 264.9452

Identification/Properties

Computed Properties
Molecular Weight:
264.948g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
264.892g/mol
Monoisotopic Mass:
262.895g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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


2-Bromo-3-(bromomethyl)-6-methylpyridine serves as a versatile building block in chemical synthesis, particularly in organic reactions where the introduction of bromine-containing groups is essential. This compound is commonly utilized as a key intermediate in the pharmaceutical industry for the synthesis of various bioactive molecules and pharmaceutical intermediates. Its unique structure enables it to participate in diverse chemical transformations, including nucleophilic substitution, palladium-catalyzed coupling reactions, and halogenation processes. Furthermore, 2-Bromo-3-(bromomethyl)-6-methylpyridine's reactivity and selectivity make it a valuable tool for the modification of complex organic molecules, enabling the preparation of novel compounds with enhanced properties and functionality.