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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, 3,5-dibromo-2,6-dimethyl-

Brc1cc(Br)c(nc1C)C Request for Quotation
Chemical Name: Pyridine, 3,5-dibromo-2,6-dimethyl-
CAS Number: 3430-34-0
Product Number: AG00C71Q(AGN-PC-0JWHWG)
Synonyms:
MDL No:
Molecular Formula: C7H7Br2N
Molecular Weight: 264.9452

Identification/Properties

Properties
MP:
68 - 69 °C
BP:
240.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
264.948g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
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:
106
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


A versatile compound in chemical synthesis, 3,5-Dibromo-2,6-dimethylpyridine, serves as a valuable building block in the creation of various compounds. This compound is known for its ability to facilitate the formation of new carbon-carbon and carbon-heteroatom bonds, making it a crucial component in the development of complex organic molecules. With its unique molecular structure, 3,5-Dibromo-2,6-dimethylpyridine plays a key role in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and specificity in chemical reactions make it an indispensable tool for chemists seeking to innovate and create novel compounds with specific properties and functionalities.