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4'-Iodoacetophenone, 98%|122146|13329-40-3

4'-Iodoacetophenone, 98%

Cat. No JK122146_5_G
J&K Chemical

Product Information

Product Name
4'-Iodoacetophenone, 98%
Brand Name
J&K
Product Number
122146
CAS
13329-40-3
Molecular Formula
C8H7IO
Molecular Weight
246.05
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
72869
IUPAC Name
1-(4-iodophenyl)ethanone
InChI Key
JZJWCDQGIPQBAO-UHFFFAOYSA-N
SMILES
CC(=O)C1=CC=C(C=C1)I

Properties

Melting Point
82-84

Safety Information

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

A single electrolyzer-making amides and α-ketoamides together: A “sweet fusion” of electrocatalysis and chemocatalysis!
Publication Name: Journal of Chemical Sciences
Publication Date: 2025-10-18
DOI: 10.1007/s12039-025-02440-4

Catalysis in Protein Cages
Publication Name: Topics in Organometallic Chemistry
Publication Date: 2025
DOI: 10.1007/3418_2025_124

Noncanonical Amino Acids in the Design of Artificial Metalloenzymes
Publication Name: Topics in Organometallic Chemistry
Publication Date: 2025
DOI: 10.1007/3418_2025_130

Benzo[c]cinnolines by Palladium(II)-Catalyzed C—H Arylation of 1-Arylhydrazine-1,2-dicarboxylates Followed by C—H Amination
Publication Name: Science of Synthesis
Publication Date: 2025

Using Chloro-Substituted Difluoroalkylating Reagents
Publication Name: Science of Synthesis
Publication Date: 2025

4'-Iodoacetophenone, 98%

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