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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)-

3,6-Pyridazinedione, 4-bromo-1,2-dihydro-

O=c1[nH][nH]c(=O)c(c1)Br Request for Quotation
Chemical Name: 3,6-Pyridazinedione, 4-bromo-1,2-dihydro-
CAS Number: 15456-86-7
Product Number: AG0037PW(AGN-PC-0JNSHG)
Synonyms:
MDL No:
Molecular Formula: C4H3BrN2O2
Molecular Weight: 190.9828

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

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


4-Bromo-1,2-dihydropyridazine-3,6-dione is a versatile chemical compound commonly used in organic synthesis for its unique properties and reactivity. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and functional materials due to its ability to serve as a precursor in the synthesis of complex molecules.In chemical synthesis, 4-Bromo-1,2-dihydropyridazine-3,6-dione can act as a valuable building block for the construction of heterocyclic compounds, which are prevalent in a wide range of bioactive molecules. Its bromine functional group allows for selective transformations and regioselective reactions, enabling the introduction of diverse substituents to tailor the structure and properties of the final products.Moreover, the presence of the dihydropyridazine ring system enhances the reactivity of 4-Bromo-1,2-dihydropyridazine-3,6-dione, making it a valuable intermediate for the synthesis of nitrogen-containing compounds. This compound can participate in various cyclization reactions, cascade reactions, and multi-step syntheses to access structurally complex molecules efficiently.Furthermore, 4-Bromo-1,2-dihydropyridazine-3,6-dione's ability to undergo functional group manipulations and provide access to diverse chemical space makes it a valuable tool for medicinal chemists, agrochemists, and material scientists. Its utility in synthesizing biologically active compounds, crop protection agents, and advanced materials highlights its significance in modern chemical research and development.In conclusion, 4-Bromo-1,2-dihydropyridazine-3,6-dione serves as a crucial building block in chemical synthesis, offering versatility, reactivity, and potential for the creation of novel molecules with tailored properties and functions. Its role in the development of advanced materials and biologically active compounds underscores its importance in pushing the boundaries of scientific innovation.