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Methyl3-hydroxy-5-iodobenzoate

Base Information
  • Chemical Name:Methyl3-hydroxy-5-iodobenzoate
  • CAS No.:50765-22-5
  • Molecular Formula:C8H7IO3
  • Molecular Weight:278.046
  • Hs Code.:2918290000
  • Mol file:50765-22-5.mol
Methyl3-hydroxy-5-iodobenzoate

Synonyms:Benzoic acid, 3-hydroxy-5-iodo-, methyl ester; Methyl 3-hydroxy-5-iodobenzoate

Suppliers and Price of Methyl3-hydroxy-5-iodobenzoate
Supply Marketing:
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
  • Methyl3-hydroxy-5-iodobenzoate
  • 25mg
  • $ 105.00
  • Crysdot
  • Methyl3-hydroxy-5-iodobenzoate 97%
  • 1g
  • $ 480.00
  • American Custom Chemicals Corporation
  • METHYL-3-HYDROXY-5-IODOBENZOATE 95.00%
  • 5MG
  • $ 496.20
  • Alichem
  • Methyl3-hydroxy-5-iodobenzoate
  • 1g
  • $ 922.18
  • AK Scientific
  • Methyl3-hydroxy-5-iodobenzoate
  • 1g
  • $ 1345.00
Total 17 raw suppliers
Chemical Property of Methyl3-hydroxy-5-iodobenzoate
Chemical Property:
  • Vapor Pressure:5.95E-06mmHg at 25°C 
  • Refractive Index:1.633 
  • Boiling Point:368.6°C at 760 mmHg 
  • Flash Point:176.7°C 
  • PSA:46.53000 
  • Density:1.88g/cm3 
  • LogP:1.78340 
  • Storage Temp.:2-8°C(protect from light) 
Purity/Quality:

97% *data from raw suppliers

Methyl3-hydroxy-5-iodobenzoate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Methyl 3-hydroxy-5-iodobenzoate
Technology Process of Methyl3-hydroxy-5-iodobenzoate

There total 4 articles about Methyl3-hydroxy-5-iodobenzoate 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 thionyl chloride; at 0 - 23 ℃; for 16.5h;
DOI:10.1021/acs.jmedchem.6b00044
Guidance literature:
Multi-step reaction with 3 steps
1: (i) SOCl2, (ii) /BRN= 1098229/
2: SnCl2, aq. HCl
3: (i) aq. NaNO2, H2SO4, (ii) aq. H2SO4
With hydrogenchloride; tin(ll) chloride;
DOI:10.1021/jm00264a023
Guidance literature:
Multi-step reaction with 2 steps
1: SnCl2, aq. HCl
2: (i) aq. NaNO2, H2SO4, (ii) aq. H2SO4
With hydrogenchloride; tin(ll) chloride;
DOI:10.1021/jm00264a023
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