Phenol, 2,6-dichloro-4-iodo-


Chemical Name: Phenol, 2,6-dichloro-4-iodo-
CAS Number: 34074-22-1
Product Number: AG00CKQH(AGN-PC-0LC412)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl2IO
Molecular Weight: 288.8979

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
288.893g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
287.861g/mol
Monoisotopic Mass:
287.861g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,6-Dichloro-4-iodophenol is a versatile compound widely used in organic synthesis due to its unique chemical properties. This compound serves as an important building block in the preparation of pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 2,6-Dichloro-4-iodophenol can act as a valuable starting material for the synthesis of various biologically active compounds and functional materials. Its strategic placement of halogen substituents allows for selective functionalization, enabling the introduction of additional functional groups with high precision. This compound is particularly valuable in medicinal chemistry and material science research, where the ability to control regioselectivity and stereochemistry is crucial for the synthesis of complex molecules. The presence of both chlorine and iodine atoms in 2,6-Dichloro-4-iodophenol imparts unique reactivity and compatibility with a variety of reaction conditions, making it a versatile intermediate in the synthesis of diverse chemical compounds.