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4-Iodophenetole, 99%|338909|699-08-1

4-Iodophenetole, 99%

Cat. No JK338909_5_G
J&K Chemical

Product Information

Product Name
4-Iodophenetole, 99%
Brand Name
J&K
Product Number
338909
CAS
699-08-1
Molecular Formula
C8H9IO
Molecular Weight
248.06
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
4-Ethoxyiodobenzene
PubChem CID
220700
IUPAC Name
1-ethoxy-4-iodobenzene
InChI Key
VSIIHWOJPSSIDI-UHFFFAOYSA-N
SMILES
CCOC1=CC=C(C=C1)I

Properties

Melting Point
25-28
Boiling Point
133-134
Flash Point
110
n20D
1.5970

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Functional modification, self-assembly and application of calix[4]resorcinarenes
Publication Name: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Publication Date: 2022-01-11
DOI: 10.1007/s10847-021-01119-w

Enantioselective Reductive Diarylation of Unactivated Alkenes
Publication Name: Science of Synthesis
Publication Date: 2022

Transthioetherification of Aryl Halides with Thioethers or Thioesters under Palladium Catalysis
Publication Name: Synfacts
Publication Date: 2020-03-18
DOI: 10.1055/s-0040-1707641

A Newly Designed Carbohydrate-Derived Alkylamine Promotes Ullmann Type C–N Coupling Catalyzed by Copper in Water
Publication Name: Synlett
Publication Date: 2018-12-17
DOI: 10.1055/s-0037-1611695

Pd- and Ni-Pyridyl Complexes Deposited as Films for Suzuki–Miyaura and Mizoroki–Heck Cross Coupling Reactions
Publication Name: Catalysis Letters
Publication Date: 2015-09-07
DOI: 10.1007/s10562-015-1614-4

4-Iodophenetole, 99%

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