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Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)-

Base Information Edit
  • Chemical Name:Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)-
  • CAS No.:54102-37-3
  • Molecular Formula:C15H14O4
  • Molecular Weight:258.274
  • Hs Code.:
  • Mol file:54102-37-3.mol
Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)-

Synonyms:

Suppliers and Price of Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)-
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
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  • price
Total 1 raw suppliers
Chemical Property of Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)- Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)-

There total 2 articles about Benzoic acid, 2-hydroxy-6-methyl-4-(phenylmethoxy)- 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 trifluoroacetic acid; In water; for 24h;
DOI:10.1016/j.tetlet.2018.10.020
Guidance literature:
Multi-step reaction with 3 steps
1: trifluoroacetic anhydride; trifluoroacetic acid / 24 h / 25 °C
2: sodium hydride / tetrahydrofuran / 6 h / 0 - 25 °C
3: trifluoroacetic acid / water / 24 h
With sodium hydride; trifluoroacetic acid; trifluoroacetic anhydride; In tetrahydrofuran; water;
DOI:10.1016/j.tetlet.2018.10.020
Guidance literature:
With sulfuryl dichloride; In diethyl ether; for 22h; Ambient temperature;
DOI:10.1071/CH9950635
Refernces Edit
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