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About This Item
Empirical Formula (Hill Notation):
C6H5I
CAS Number:
Molecular Weight:
204.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-719-6
Beilstein/REAXYS Number:
1446140
MDL number:
Assay:
98%
Quality Level
assay
98%
refractive index
n20/D 1.62 (lit.)
bp
188 °C (lit.)
mp
−29 °C (lit.)
density
1.823 g/mL at 25 °C (lit.)
SMILES string
Ic1ccccc1
InChI
1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H
InChI key
SNHMUERNLJLMHN-UHFFFAOYSA-N
General description
Iodobenzene, also known as phenyl iodide, is commonly used as an arylating agent in various cross-coupling reactions.
Application
Iodobenzene is used in various C-C coupling reactions. It can be used in the preparation of iodobenzene dichloride, which is employed as an oxidant to oxidize alcohols to carbonyl compounds and as a chlorinating agent.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
170.6 °F - closed cup
flash_point_c
77 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Articles
Our strategy is to synthesize mesoporous carbonaceous materials (“Starbons”) using mesoporous expanded starch as the precursor without the need for a templating agent.
Ring-Opening 1, 3-Dichlorination of Donor-Acceptor Cyclopropanes by Iodobenzene Dichloride.
Garve, Lennart KB et al.
Organic Letters, 16(21), 5804-5807 (2014)
Catalysis by gold (I) and gold (III): a parallelism between homo-and heterogeneous catalysts for copper-free Sonogashira cross-coupling reactions.
Gonzalez-Arellano, Camino et al.
Angewandte Chemie (International Edition in English), 46(9), 1536-1538 (2007)
Iodobenzene dichloride as a stoichiometric oxidant for the conversion of alcohols into carbonyl compounds; two facile methods for its preparation.
Zhao, Xue-Fei and Zhang, Chi
Synthesis, 2007(04), 551-557 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I7632-5G-A | 04061833858318 |
| I7632-500G-A | 04061832677064 |
| I7632-100G-A | 04061833858301 |
