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Benzoic acid, 2-ethyl-4,6-dihydroxy-

Base Information Edit
  • Chemical Name:Benzoic acid, 2-ethyl-4,6-dihydroxy-
  • CAS No.:4299-73-4
  • Molecular Formula:C9H10O4
  • Molecular Weight:182.176
  • Hs Code.:2918290000
  • Mol file:4299-73-4.mol
Benzoic acid, 2-ethyl-4,6-dihydroxy-

Synonyms:2,4-Dihydroxy-6-ethylbenzoesaeure;

Suppliers and Price of Benzoic acid, 2-ethyl-4,6-dihydroxy-
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
  • 2-Ethyl-4,6-dihydroxybenzoicacid
  • 100mg
  • $ 605.00
  • TRC
  • 2-Ethyl-4,6-dihydroxybenzoicacid
  • 25mg
  • $ 160.00
  • A1 Biochem Labs
  • 2-Ethyl-4,6-dihydroxybenzoicacid 95%
  • 200 mg
  • $ 800.00
Total 2 raw suppliers
Chemical Property of Benzoic acid, 2-ethyl-4,6-dihydroxy- Edit
Chemical Property:
  • PSA:77.76000 
  • LogP:1.35840 
Purity/Quality:

95% *data from raw suppliers

2-Ethyl-4,6-dihydroxybenzoicacid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 2-Ethyl-4,6-dihydroxybenzoic acid is a useful compound that is used in hair dye products.
Technology Process of Benzoic acid, 2-ethyl-4,6-dihydroxy-

There total 15 articles about Benzoic acid, 2-ethyl-4,6-dihydroxy- 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 aluminium trichloride; In chlorobenzene; for 0.75h; Heating;
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) lithium / multistep reaction; other n-alkyl-lithium compounds; no 6-ethyl-2,4-dimethoxybenzoic acid from 2,4-dimethoxyfluorobenzene in the same conditions; 3,5-dimethoxybenzyne intermediate
2: 63 percent / aluminium chloride / chlorobenzene / 0.75 h / Heating
With aluminium trichloride; lithium; In chlorobenzene;
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