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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)-

Benzene, 1,4-dichloro-2-iodo-

Clc1ccc(c(c1)I)Cl Request for Quotation
Chemical Name: Benzene, 1,4-dichloro-2-iodo-
CAS Number: 29682-41-5
Product Number: AG002Z4A(AGN-PC-0JLNXX)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl2I
Molecular Weight: 272.8985

Identification/Properties

Properties
MP:
21 °C(lit.)
BP:
255.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Stability:
Light Sensitive
Refractive Index:
n20/D 1.646(lit.)
Computed Properties
Molecular Weight:
272.894g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
271.866g/mol
Monoisotopic Mass:
271.866g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
97.1
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:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1,4-Dichloro-2-iodobenzene compound is a versatile building block widely utilized in organic chemical synthesis due to its unique reactivity and functional group compatibility. Its application in various synthetic processes allows for the efficient formation of complex molecules with specific structural features.1,4-Dichloro-2-iodobenzene is commonly employed as a halogenated aryl iodide electrophile in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings. These reactions enable the selective and controlled introduction of the 1,4-dichloro-2-iodobenzene moiety into larger molecular frameworks, facilitating the construction of biaryl compounds, pharmaceutical intermediates, agrochemicals, and materials with desired properties.Additionally, the unique combination of chlorine and iodine substituents in 1,4-Dichloro-2-iodobenzene allows for further diversification via selective substitution or elimination reactions. The presence of electron-withdrawing chloro groups enhances the reactivity and ortho directing ability of the iodine atom, making it a valuable precursor for functional group transformations and regioselective syntheses.Overall, the strategic incorporation of 1,4-Dichloro-2-iodobenzene in chemical synthesis offers chemists a powerful tool to access a wide range of structurally diverse and synthetically challenging molecules, highlighting its significance in the modern organic chemistry toolbox.