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2-Iodoanisole

CAS No.
529-28-2
Chemical Name:
2-Iodoanisole
Synonyms
1-IODO-2-METHOXYBENZENE;Iodanisol;O-IODOANISOLE;2-IODOANISOLE;o-Anisyl iodide;2-Iodoanisole97%;Anisole, o-iodo-;2-Iodoanisole 97%;2-Iodoanisole,99%;2-Iodoanisole 
CBNumber:
CB7161179
Molecular Formula:
C7H7IO
Molecular Weight:
234.03
MDL Number:
MFCD00001039
MOL File:
529-28-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:30:15

2-Iodoanisole Properties

Melting point 588.5 °C
Boiling point 125-126 °C19 mm Hg(lit.)
Density 1.799 g/mL at 25 °C(lit.)
refractive index n20/D 1.622(lit.)
Flash point >110°C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility alcohol: miscible(lit.)
form Liquid
color Clear yellow
Specific Gravity 1.799
Water Solubility insoluble
Sensitive Light Sensitive
Merck 14,5028
BRN 1860243
InChI 1S/C7H7IO/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3
InChIKey DVQWNQBEUKXONL-UHFFFAOYSA-N
SMILES COc1ccccc1I
CAS DataBase Reference 529-28-2(CAS DataBase Reference)
FDA UNII 75Y5532R8O
NIST Chemistry Reference 2-Iodoanisole(529-28-2)
EPA Substance Registry System Benzene, 1-iodo-2-methoxy- (529-28-2)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
8
TSCA  TSCA listed
HS Code  29093090
Storage Class 10 - Combustible liquids
NFPA 704
1
2 0

2-Iodoanisole price More Price(66)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 252786 2-Iodoanisole 98% 529-28-2 25g $64.7 2026-04-30 Buy
Sigma-Aldrich 252786 2-Iodoanisole 98% 529-28-2 100g $162 2026-04-30 Buy
TCI Chemical I0382 2-Iodoanisole (stabilized with Copper chip) >98.0%(GC) 529-28-2 25g $58 2026-04-30 Buy
TCI Chemical I0382 2-Iodoanisole (stabilized with Copper chip) min.98.0% 529-28-2 100G $158 2026-04-30 Buy
Usbiological 280921 1-Iodo-2-methoxybenzene Asreported 529-28-2 100g $355 2026-06-03 Buy
Product number Packaging Price Buy
252786 25g $64.7 Buy
252786 100g $162 Buy
I0382 25g $58 Buy
I0382 100G $158 Buy
280921 100g $355 Buy

2-Iodoanisole Chemical Properties, Uses, Production

Chemical Properties

Clear yellow liquid

Uses

suzuki reaction

Uses

2-Iodoanisole has been used in palladium/copper-catalyzed synthesis of o-(1-alkynyl)anisoles.

Definition

ChEBI: An organoiodine compound that is iodobenzene substituted by methoxy group at psotion 2.

General Description

2-Iodoanisole participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.

Synthesis

(1) Prepare 2 moles of 20% NaI aqueous solution A and 2.1 moles of 8-10% sodium hypochlorite aqueous solution B for spare use;

(2) Add 900g of anisole in a 2L four-necked round-bottomed flask equipped with stirring, a temperature display, and two constant-pressure dropping funnels and heat it up to 60-70C with stirring; then, dropwise add the sodium iodide solution and sodium hypochlorite solution simultaneously at the ratio of molar ratio 1:1.05 with stirring;

(3) After dropping and adding, warm it up to 75-80C and get the light yellow reaction solution; cool it down to 75-80C; and cool it down to 80%. Sodium iodide solution and sodium hypochlorite solution;

(3) after dropping, warm up to 75~80 , stirring for 1 hour, to get light yellow reaction solution; cooled to room temperature, static phase splitting; the organic phase washed with water, drying and filtration, to get the anisole solution of 2-iodoanisole, distillation, cooling, curing, to get the white lumpy crystals, i.e., 2-iodoanisole, whose content is 98.5%, yield 93.4% .

Global Suppliers ( 288)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Beijing HwrkChemical Technology Co., Ltd 89508211 18501085097 sales.bj@hwrkchemical.com China 9407 55
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
Beijing Ouhe Technology Co., Ltd 13552068683 13522913783 2355560935@qq.com China 11777 60
JinYan Chemicals(ShangHai) Co.,Ltd. 13817811078 sales@jingyan-chemical.com China 9963 60
Shanghai Sinch Parmaceuticals Tech. Co. Ltd. +86-21-54098501 sales@sinch.com.cn China 11592 64

View Latest Price from 2-Iodoanisole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Iodoanisole pictures 2019-08-06 2-Iodoanisole
529-28-2
$1.00 1KG 98% 150KG Career Henan Chemical Co
1-Iodo-2-methoxybenzene, 2-Iodophenyl methyl ether Adjacent iodine benzene Methyl ether 2-IODOANISOLE O-IODOANISOLE 1-iodo-2-methoxy-benzen Anisole, o-iodo- Benzene, 1-iodo-2-methoxy- Iodanisol o-Anisyl iodide 2-iodophenyl methyl ether 2-Iodoanisole97% 2-Iodoanisole 97% 2-Iodoanisole,99% 2-methoxyiodobenzene 2-IODOANISOLE / 1-IODO-2-METHOXYBENZENE 2-Iodoanisole (stabilized with Copper chip) 2-Iodophenyl methyl ether, 2-Methoxyiodobenzene o-Iodomethoxybenzene o-Methoxyiodobenzene 1-Methoxy-2-iodobenzene 2-Iodo-1-methoxybenzene 2-Methoxyphenyl iodide 2-Iodoanisole o-Iodoanisole 2-Iodoanisole,2-Iodophenyl methyl ether, 2-Methoxyiodobenzene 2-Iodoanisole  2-Iodoanisole, 97% 5GR 2-Iodoanisole(stabilizedwithCopperchip)> 2-iodobenzene methyl ether (2-iodobenzene methyl ether) 1-IODO-2-METHOXYBENZENE 529-28-2 C7H7IO Organic Building Blocks Ethers Oxygen Compounds ETHER Building Blocks Building Blocks C2 to C8 Chemical Synthesis Ethers Organic Building Blocks Oxygen Compounds Aromatic Ethers Anisole Anisoles, Alkyloxy Compounds & Phenylacetates Iodine Compounds alkyl Iodine