| Identification | More | [Name]
2-Iodoanisole | [CAS]
529-28-2 | [Synonyms]
1-IODO-2-METHOXYBENZENE
2-IODOANISOLE
O-IODOANISOLE
1-iodo-2-methoxy-benzen
Anisole, o-iodo-
Benzene, 1-iodo-2-methoxy-
Iodanisol
o-Anisyl iodide
2-Iodoanisole97%
2-Iodoanisole 97%
2-Iodoanisole,99%
2-iodophenyl methyl ether
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 | [EINECS(EC#)]
208-456-4 | [Molecular Formula]
C7H7IO | [MDL Number]
MFCD00001039 | [Molecular Weight]
234.03 | [MOL File]
529-28-2.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear yellow liquid | [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.)
| [Fp ]
>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 | [CAS DataBase Reference]
529-28-2(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Iodoanisole(529-28-2) | [EPA Substance Registry System]
529-28-2(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
8 | [TSCA ]
Yes | [HS Code ]
29093090 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear yellow liquid | [Uses]
2-Iodoanisole has been used in palladium/copper-catalyzed synthesis of o-(1-alkynyl)anisoles. | [Uses]
suzuki reaction | [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. |
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