2-Iodo-4-acetylphenol

CAS No.
62615-24-1
Chemical Name:
2-Iodo-4-acetylphenol
Synonyms
2-Iodo-4-acetylphenol;4-Acetyl-2-iodophenol;4'-Hydroxy-3'-iodoacetophenone;3'-Iodo-4'-hydroxyacetophenone;4'-Hydroxy-3'-iodoacetophenone 97%;1-(4-Hydroxy-3-iodo-phenyl)-ethanone;Ethanone, 1-(4-hydroxy-3-iodophenyl)-
CBNumber:
CB82367833
Molecular Formula:
C8H7IO2
Molecular Weight:
262.04
MDL Number:
MFCD06200221
MOL File:
62615-24-1.mol
MSDS File:
SDS
Last updated:2022-08-15 17:41:11

2-Iodo-4-acetylphenol Properties

Melting point 155-160°C

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H318
Precautionary statements  P280-P301+P312+P330-P305+P351+P338+P310
Hazard Codes  Xn
Risk Statements  22-41
Safety Statements  26-39
WGK Germany  1

2-Iodo-4-acetylphenol price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 722057 4′-Hydroxy-3′-iodoacetophenone 97% 62615-24-1 5g $135 2024-03-01 Buy
AK Scientific 1108AQ 4′-Hydroxy-3′-iodoacetophenone 62615-24-1 5g $190 2021-12-16 Buy
American Custom Chemicals Corporation HCH0066522 4'-HYDROXY-3'-IODOACETOPHENONE 95.00% 62615-24-1 5G $897.44 2021-12-16 Buy
Chemcia Scientific BB20-7542 1-(4-Hydroxy-3-iodo-phenyl)-ethanone 95% 62615-24-1 0.5g $265 2021-12-16 Buy
Product number Packaging Price Buy
722057 5g $135 Buy
1108AQ 5g $190 Buy
HCH0066522 5G $897.44 Buy
BB20-7542 0.5g $265 Buy

2-Iodo-4-acetylphenol Chemical Properties,Uses,Production

Uses

Reactant for:

  • Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes
  • Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction
  • Regioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in air
  • Preparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclization
  • Stereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenes
  • Preparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynes
  • Preparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina

Preparation

Preparation by reaction of iodine and potassium iodide on 4-hydroxyacetophenone in aqueous ammonium hydroxide at r.t. (54–57%).

Synthesis Reference(s)

Journal of Medicinal Chemistry, 23, p. 738, 1980 DOI: 10.1021/jm00181a008

2-Iodo-4-acetylphenol Preparation Products And Raw materials

2-Iodo-4-acetylphenol Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
sgtlifesciences pvt ltd
+8617013299288 dj@sgtlifesciences.com China 12382 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
SuZhou ShiYa Biopharmaceuticals, Inc. 0512-52358471 17715136450 sales@shiyabiopharm.com China 13502 58
Zhuhai Aobokai Biomedical Technology Co., Ltd. 400-0628126 15697568815; sales-team@aobchem.com.cn China 20186 58
Shaanxi Dideu Medichem Co. Ltd 029-81124267 15229202216 1073@dideu.com China 10011 58
Shanghai Aladdin Biochemical Technology Co.,Ltd. +86-18521732826 market@aladdin-e.com China 48617 58
2-Iodo-4-acetylphenol 3'-Iodo-4'-hydroxyacetophenone 4'-Hydroxy-3'-iodoacetophenone 4'-Hydroxy-3'-iodoacetophenone 97% 4-Acetyl-2-iodophenol Ethanone, 1-(4-hydroxy-3-iodophenyl)- 1-(4-Hydroxy-3-iodo-phenyl)-ethanone 62615-24-1