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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)-

3,5-dibromo-2-methylpyridin-4-amine

Brc1cnc(c(c1N)Br)C Request for Quotation
Chemical Name: 3,5-dibromo-2-methylpyridin-4-amine
CAS Number: 126325-54-0
Product Number: AG000SKE(AGN-PC-001CZC)
Synonyms:
MDL No:
Molecular Formula: C6H6Br2N2
Molecular Weight: 265.9332

Identification/Properties

Computed Properties
Molecular Weight:
265.936g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
265.888g/mol
Monoisotopic Mass:
263.89g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dibromo-2-methylpyridin-4-amine is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various heterocyclic molecules. Its unique structure and reactivity make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as a crucial starting material in the development of new synthetic pathways and strategies for creating complex organic compounds. Its presence enables chemists to access a diverse range of functionalized molecules with different biological activities and properties. In chemical synthesis, 3,5-Dibromo-2-methylpyridin-4-amine plays a vital role in facilitating the efficient and strategic assembly of complex molecular structures by serving as a key component in diverse synthetic transformations and functional group modifications. Its utility in various synthetic methodologies highlights its importance as a valuable tool for organic chemists seeking to explore new avenues in the creation of novel compounds and materials.