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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)-

Pyridazine, 3-iodo-6-methyl-

Cc1ccc(nn1)I Request for Quotation
Chemical Name: Pyridazine, 3-iodo-6-methyl-
CAS Number: 1618-47-9
Product Number: AG001VX1(AGN-PC-0NJVG8)
Synonyms:
MDL No:
Molecular Formula: C5H5IN2
Molecular Weight: 220.0111

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
220.013g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
219.95g/mol
Monoisotopic Mass:
219.95g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
76.8
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-Iodo-6-methylpyridazine is a versatile compound that finds application in several key areas of chemical synthesis. In particular, its unique structure and reactivity make it a valuable building block for the creation of various pharmaceuticals, agrochemicals, and materials.One prominent use of 3-Iodo-6-methylpyridazine is as a key intermediate in the synthesis of novel heterocyclic compounds. Its ability to undergo various functionalization reactions, such as cross-coupling and substitution reactions, allows for the efficient construction of complex molecular structures. This capability is crucial in medicinal chemistry, where the development of new drug candidates often relies on the synthesis of diverse heterocyclic scaffolds.Additionally, 3-Iodo-6-methylpyridazine serves as a valuable precursor for the introduction of functional groups and substitution patterns into organic molecules. By strategically utilizing the iodine atom as a handle for further transformations, chemists can tailor the properties of the final compounds for specific applications. This versatility makes 3-Iodo-6-methylpyridazine a valuable tool in the design and synthesis of advanced materials and specialty chemicals.Furthermore, the presence of both the iodine and methyl substituents on the pyridazine ring imparts unique reactivity and selectivity profiles to 3-Iodo-6-methylpyridazine. These characteristics enable chemists to fine-tune the regio- and stereochemistry of the products, facilitating the synthesis of target molecules with high efficiency and purity.In conclusion, 3-Iodo-6-methylpyridazine plays a crucial role in modern chemical synthesis, offering a wide range of applications in the construction of complex organic molecules. Its versatility, reactivity, and functional group compatibility make it a valuable tool for researchers and synthetic chemists striving to develop innovative compounds for various industries.