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5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID

Base Information Edit
  • Chemical Name:5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID
  • CAS No.:157436-33-4
  • Molecular Formula:C12H14O5
  • Molecular Weight:238.24
  • Hs Code.:
  • Mol file:157436-33-4.mol
5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID

Synonyms:5-tert-butyl-2-hydroxybenzene-1,3-dioic acid

Suppliers and Price of 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID
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
  • American Custom Chemicals Corporation
  • 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID 95.00%
  • 5MG
  • $ 687.35
  • American Custom Chemicals Corporation
  • 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID 95.00%
  • 10MG
  • $ 679.14
  • American Custom Chemicals Corporation
  • 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID 95.00%
  • 1MG
  • $ 647.61
Total 2 raw suppliers
Chemical Property of 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID

There total 4 articles about 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALIC ACID 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 hydrogen bromide; In acetic acid; at 120 ℃; for 0.166667h;
DOI:10.1002/hlca.19980810304
Guidance literature:
With tert-butylbenzene; n-heptane; n-pentylsodium; anschliessendes Umsetzen mit CO2;
DOI:10.1021/ja01648a052
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / K2CO3 / acetone / 18 h / Heating
2: 97 percent / NaOH, Adogen 464, KMnO4 / H2O / 50 degC, 1 h, reflux, 5 min
3: 77 percent / HBr / acetic acid / 0.17 h / 120 °C
With sodium hydroxide; potassium permanganate; adogen 464; hydrogen bromide; potassium carbonate; In water; acetic acid; acetone;
DOI:10.1002/hlca.19980810304
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