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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, 2,3-dibromo-6-methyl-

Cc1ccc(c(n1)Br)Br Request for Quotation
Chemical Name: Pyridine, 2,3-dibromo-6-methyl-
CAS Number: 261373-04-0
Product Number: AG002RTH(AGN-PC-03NA42)
Synonyms:
MDL No:
Molecular Formula: C6H5Br2N
Molecular Weight: 250.9186

Identification/Properties

Computed Properties
Molecular Weight:
250.921g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
250.877g/mol
Monoisotopic Mass:
248.879g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
97.1
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

Request for Quotation

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Chemical Structure


2,3-Dibromo-6-picoline is a valuable chemical compound widely used in organic synthesis. This compound has applications in various chemical reactions, particularly in the field of heterocyclic chemistry. It serves as a versatile building block for the synthesis of complex organic molecules and pharmaceuticals.The presence of bromine atoms on the picoline ring provides unique reactivity that allows 2,3-Dibromo-6-picoline to participate in a range of substitution and coupling reactions. These reactions can be used to introduce diverse functional groups into the molecule, enabling the creation of new compounds with specific properties and applications.2,3-Dibromo-6-picoline plays a crucial role in the preparation of pharmaceutical intermediates, agrochemicals, and advanced materials. Its ability to undergo selective transformations makes it a valuable tool for organic chemists seeking to design and synthesize novel molecules with desired biological or physical properties.In summary, 2,3-Dibromo-6-picoline is a versatile building block in chemical synthesis, enabling the creation of complex organic compounds with applications across various industries.