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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, 3,6-diiodo-

Ic1ccc(nn1)I Request for Quotation
Chemical Name: Pyridazine, 3,6-diiodo-
CAS Number: 20698-04-8
Product Number: AG002IRH(AGN-PC-0JNPLE)
Synonyms:
MDL No:
Molecular Formula: C4H2I2N2
Molecular Weight: 331.8810

Identification/Properties

Computed Properties
Molecular Weight:
331.883g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
331.831g/mol
Monoisotopic Mass:
331.831g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
68.4
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


Pyridazine, 3,6-diiodo- is a versatile compound that plays a crucial role in chemical synthesis. Due to its unique molecular structure and reactivity, this compound is commonly used as a building block in the synthesis of various organic compounds. One of the key applications of Pyridazine, 3,6-diiodo- is its use as a powerful electrophilic iodinating reagent in chemical transformations. It can efficiently introduce iodine atoms onto organic molecules, allowing for the selective modification of functional groups. This property makes it valuable in the synthesis of complex molecules and pharmaceutical intermediates. Furthermore, Pyridazine, 3,6-diiodo- serves as a useful synthetic tool in cross-coupling reactions, where it can facilitate the formation of carbon-carbon or carbon-heteroatom bonds. Its ability to act as a versatile coupling partner enhances the scope and efficiency of various synthetic methodologies, contributing to the development of new and innovative chemical processes.Overall, Pyridazine, 3,6-diiodo- is a valuable compound in chemical synthesis, offering unique reactivity and versatility for the efficient construction of complex organic molecules and materials.