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4-HYDROXY-3-IODOBENZYL ALCOHOL

Base Information Edit
  • Chemical Name:4-HYDROXY-3-IODOBENZYL ALCOHOL
  • CAS No.:197230-74-3
  • Molecular Formula:C7H7IO2
  • Molecular Weight:250.036
  • Hs Code.:
  • Mol file:197230-74-3.mol
4-HYDROXY-3-IODOBENZYL ALCOHOL

Synonyms:4-HYDROXY-3-IODOBENZYL ALCOHOL;4-(hydroxymethyl)-2-iodophenol;BENZENEMETHANOL,4-HYDROXY-3-IODO-;T3 intermediates

Suppliers and Price of 4-HYDROXY-3-IODOBENZYL ALCOHOL
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 4-(Hydroxymethyl)-2-iodophenol
  • 5g
  • $ 430.00
  • Labseeker
  • BENZENEMETHANOL,4-HYDROXY-3-IODO- 95
  • 5g
  • $ 1633.00
  • Labseeker
  • BENZENEMETHANOL,4-HYDROXY-3-IODO- 95
  • 1g
  • $ 1250.00
  • Chemcia Scientific
  • 4-Hydroxymethyl-2-iodo-phenol >97%
  • 0.5 G
  • $ 195.00
  • American Custom Chemicals Corporation
  • 4-HYDROXY-3-IODOBENZYL ALCOHOL 95.00%
  • 5MG
  • $ 503.62
Total 6 raw suppliers
Chemical Property of 4-HYDROXY-3-IODOBENZYL ALCOHOL Edit
Chemical Property:
  • PSA:40.46000 
  • LogP:1.48910 
  • Storage Temp.:Refrigerator, under inert atmosphere 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

≥99.0% *data from raw suppliers

4-(Hydroxymethyl)-2-iodophenol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 4-(Hydroxymethyl)-2-iodophenol is a reagent that is used in the synthesis of 3,3’,5-Triiodo-D-thyronine (T795375), which has been shown to reduce cholesterol in blood serum.
Technology Process of 4-HYDROXY-3-IODOBENZYL ALCOHOL

There total 2 articles about 4-HYDROXY-3-IODOBENZYL ALCOHOL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With diisobutylaluminium hydride; In dichloromethane; at -78 - 20 ℃; for 2.5h; Inert atmosphere; Schlenk technique;
Guidance literature:
With ammonium peroxydisulfate; potassium iodide; In methanol; water; at 20 ℃;
DOI:10.1055/s-0029-1218698
Guidance literature:
With Pd-Cu/C; ethanolamine; triphenylphosphine; In water; at 80 ℃; for 20h; Sealed tube; Inert atmosphere;
DOI:10.3762/bjoc.9.160
Refernces Edit
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