Skip to Content
Merck
All Photos(3)

Documents

I7608

Sigma-Aldrich

4-Iodoanisole

98%

Synonym(s):

4-Iodophenyl methyl ether, 4-Methoxyiodobenzene

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
IC6H4OCH3
CAS Number:
696-62-8
Molecular Weight:
234.03
Beilstein:
1906692
EC Number:
211-798-7
MDL number:
MFCD00001056
UNSPSC Code:
12352100
PubChem Substance ID:
24896119
NACRES:
NA.22

Quality Level

100

Assay

98%

bp

237 °C/726 mmHg (lit.)

mp

50-53 °C (lit.)

SMILES string

COc1ccc(I)cc1

InChI

1S/C7H7IO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3

InChI key

SYSZENVIJHPFNL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

George W Kabalka et al.
Nuclear medicine and biology, 29(8), 841-843 (2002-11-28)
Arylboronate esters are converted to iodine-123 labeled aryl iodides using no-carrier-added iodine-123 labeled sodium iodide in the presence of chloramine-T. High yields of radiochemically pure products are obtained.
[Studies on the effect of 3 varieties of an anti-adhesive mineral oil izoform on the skin of mice].
J Rubisz-Brzezińska et al.
Przeglad dermatologiczny, 67(5), 573-580 (1980-09-01)
P N Rizk et al.
Xenobiotica; the fate of foreign compounds in biological systems, 25(2), 143-150 (1995-02-01)
1. The oxidative metabolism of 4-iodoanisole (1) by liver microsomes from beta-naphthoflavone-treated rats yields 4-iodophenol (2) 2-iodo-5-methoxyphenol (3), 2-methoxy-5-iodophenol (4), 4-methoxyphenol (5), and 3-methoxyphenol (6) in relative yields of 5:2:4:1:1 respectively. 2. [3 5-2H2]-1 was converted to the same five
M Arivazhagan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 113, 236-249 (2013-06-04)
The solid phase FT-IR and FT-Raman spectra of P-iodoanisole (P-IA) have been recorded in the regions 400-4000 and 50-4000 cm(-1), respectively. The spectra were interpreted in terms of fundamentals modes, combination and overtone bands. The structure of the molecule was

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service