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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-Amino-6-bromo-2-methylpyrimidine

Nc1cc(Br)nc(n1)C Request for Quotation
Chemical Name: 4-Amino-6-bromo-2-methylpyrimidine
CAS Number: 1161763-15-0
Product Number: AG000BTF(AGN-PC-0BL83O)
Synonyms:
MDL No:
Molecular Formula: C5H6BrN3
Molecular Weight: 188.0252

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound that plays a crucial role in chemical synthesis. Specifically, 4-Amino-6-bromo-2-methylpyrimidine is widely utilized as a key building block in the creation of various pharmaceutical and agrochemical compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of specialized substances with important biological activities.This compound's presence in chemical reactions facilitates the formation of complex molecular structures, allowing for the development of innovative drugs, pesticides, and other biologically active molecules. Through strategic manipulation of its chemical properties, 4-Amino-6-bromo-2-methylpyrimidine serves as a crucial foundation for the creation of potent compounds that exhibit targeted effects in diverse applications.Chemists and researchers rely on the strategic incorporation of 4-Amino-6-bromo-2-methylpyrimidine into their synthesis routes to access a wide range of functionalized molecules with tailored properties. By harnessing the synthetic potential of this key intermediate, scientists can efficiently access novel compounds that have the potential to drive advancements in the fields of medicine and agriculture.