337358
4-Iodo-2-methylphenol
97%
Synonym(s):
4-Iodo-o-cresol
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About This Item
Linear Formula:
IC6H3(CH3)OH
CAS Number:
Molecular Weight:
234.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C7H7IO/c1-5-4-6(8)2-3-7(5)9/h2-4,9H,1H3
SMILES string
Cc1cc(I)ccc1O
InChI key
WSBDSSKIWDFOBQ-UHFFFAOYSA-N
assay
97%
bp
105-110 °C/2 mmHg (lit.)
mp
67-68 °C (lit.)
functional group
iodo
Quality Level
Related Categories
General description
4-Iodo-2-methylphenol was prepared by direct iodination of 2-methylphenol in aqueous alcohol solvents by the action of a reagent prepared in situ from sodium hypochlorite and sodium iodide.
Application
4-Iodo-2-methylphenol was used as starting reagent in the synthesis of an agonist for the peroxisome proliferator-activated receptor δ (PPARδ) GW501516, a potential antiobesity drug.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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An efficient and selective method for the preparation of iodophenols.
Edgar KJ and Falling SN.
The Journal of Organic Chemistry, 55(18), 5287-5291 (1990)
A highly efficient synthesis of antiobestic ligand GW501516 for the peroxisome proliferator-activated receptor d through in situ protection of the phenol group by reaction with a Grignard reagent.
Ham J and Kang H.
Tetrahedron Letters, 46(39), 6683-6686 (2005)
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