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2,4-DIHYDROXY-5-METHYLBENZOIC ACID

Base Information Edit
  • Chemical Name:2,4-DIHYDROXY-5-METHYLBENZOIC ACID
  • CAS No.:4780-64-7
  • Molecular Formula:C8H8 O4
  • Molecular Weight:168.149
  • Hs Code.:
  • Mol file:4780-64-7.mol
2,4-DIHYDROXY-5-METHYLBENZOIC ACID

Synonyms:b-Resorcylic acid, 5-methyl-(7CI,8CI); 2,4-Dihydroxy-5-methylbenzoic acid

Suppliers and Price of 2,4-DIHYDROXY-5-METHYLBENZOIC 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
  • TRC
  • 2,4-Dihydroxy-5-methylbenzoicAcid
  • 250mg
  • $ 575.00
  • TRC
  • 2,4-Dihydroxy-5-methylbenzoicAcid
  • 50mg
  • $ 120.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-5-methylbenzoic acid
  • 2 g
  • $ 250.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-5-methylbenzoic acid
  • 1 g
  • $ 150.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-5-methylbenzoic acid
  • 500 mg
  • $ 100.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-5-methylbenzoic acid
  • 250 mg
  • $ 62.50
  • American Custom Chemicals Corporation
  • 2,4-DIHYDROXY-5-METHYLBENZOIC ACID 95.00%
  • 5MG
  • $ 497.94
Total 3 raw suppliers
Chemical Property of 2,4-DIHYDROXY-5-METHYLBENZOIC ACID Edit
Chemical Property:
  • Vapor Pressure:4.63E-07mmHg at 25°C 
  • Boiling Point:398.3°Cat760mmHg 
  • Flash Point:208.9°C 
  • PSA:77.76000 
  • Density:1.46g/cm3 
  • LogP:1.10440 
Purity/Quality:

2,4-Dihydroxy-5-methylbenzoicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2,4-Dihydroxy-5-methylbenzoic acid is a useful reagent in the preparation of substituted dihydroxybenzoic acids which are potential antiinflammatory agents.
Technology Process of 2,4-DIHYDROXY-5-METHYLBENZOIC ACID

There total 4 articles about 2,4-DIHYDROXY-5-METHYLBENZOIC 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 potassium hydrogencarbonate; In water; at 85 ℃; for 6h;
Guidance literature:
Multi-step reaction with 2 steps
1: hydrogenchloride; sodium cyanoborohydride / tetrahydrofuran / 3 h / 20 °C
2: potassium hydrogencarbonate / water / 6 h / 85 °C
With hydrogenchloride; sodium cyanoborohydride; potassium hydrogencarbonate; In tetrahydrofuran; water;
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