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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-(3-Bromoimidazo[1,2-b]pyridazin-6-yl)morpholine

Brc1cnc2n1nc(cc2)N1CCOCC1 Request for Quotation
Chemical Name: 4-(3-Bromoimidazo[1,2-b]pyridazin-6-yl)morpholine
CAS Number: 1012343-72-4
Product Number: AG000404(AGN-PC-0BHSDL)
Synonyms:
MDL No:
Molecular Formula: C10H11BrN4O
Molecular Weight: 283.1245

Identification/Properties

Computed Properties
Molecular Weight:
283.129g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
282.012g/mol
Monoisotopic Mass:
282.012g/mol
Topological Polar Surface Area:
42.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
249
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Bromoimidazo[1,2-b]pyridazin-6-yl)morpholine is a versatile compound commonly used in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 4-(3-Bromoimidazo[1,2-b]pyridazin-6-yl)morpholine can be utilized as a key intermediate in the preparation of biologically active molecules. Its specific structure provides opportunities for functional group transformations and allows for the introduction of diverse substituents to fine-tune the properties of the final product.Furthermore, this compound exhibits a high degree of stability under typical reaction conditions, making it an attractive choice for incorporation into synthetic pathways. Its morpholine moiety imparts solubility and potential for interactions with biological targets, making it a valuable tool in medicinal chemistry for drug discovery efforts.Overall, the application of 4-(3-Bromoimidazo[1,2-b]pyridazin-6-yl)morpholine in chemical synthesis enables the efficient and strategic construction of complex molecules with tailored properties, fostering innovation in the realms of pharmaceutical and materials science.