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3,4-DiMethyl-5-pentyl-2-furannonanoic Acid

Base Information Edit
  • Chemical Name:3,4-DiMethyl-5-pentyl-2-furannonanoic Acid
  • CAS No.:57818-40-3
  • Molecular Formula:C20H34O3
  • Molecular Weight:322.48200
  • Hs Code.:
  • Mol file:57818-40-3.mol
3,4-DiMethyl-5-pentyl-2-furannonanoic Acid

Synonyms:2-Furannonanoic acid,3,4-dimethyl-5-pentyl;10,13-epoxy-11,12-dimethyl-10,12-octadecadienoic acid;

Suppliers and Price of 3,4-DiMethyl-5-pentyl-2-furannonanoic 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
  • 3,4-Dimethyl-5-pentyl-2-furannonanoicAcid
  • 5mg
  • $ 1265.00
Total 0 raw suppliers
Chemical Property of 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid Edit
Chemical Property:
  • PSA:50.44000 
  • LogP:5.98690 
  • Storage Temp.:Amber Vial, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Dichloromethane (Slightly), Methanol (Slightly) 
Purity/Quality:

3,4-Dimethyl-5-pentyl-2-furannonanoicAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 3,4-Dimethyl-5-pentyl-2-furannonanoic acid is also known as F3 furan fatty acid. Furan fatty acids are generated in large amounts in algae and fish, but they are also produced by plants and microorganisms. Furan fatty acids exhibit radical-scavenging ability and anti-inflammatory properties.
Technology Process of 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid

There total 3 articles about 3,4-DiMethyl-5-pentyl-2-furannonanoic 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:
Multi-step reaction with 2 steps
1: 25.7 percent / SnCl4 / CHCl3 / 6 h / -50 °C
2: hydrazinhydrate, KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating
With potassium hydroxide; hydrazine hydrate; tin(IV) chloride; In chloroform; diethylene glycol;
DOI:10.1002/hlca.19850680615
Guidance literature:
Multi-step reaction with 2 steps
1: 25.7 percent / SnCl4 / CHCl3 / 6 h / -50 °C
2: hydrazinhydrate, KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating
With potassium hydroxide; hydrazine hydrate; tin(IV) chloride; In chloroform; diethylene glycol;
DOI:10.1002/hlca.19850680615
Guidance literature:
With potassium hydroxide; hydrazine hydrate; In diethylene glycol; for 1h; Heating;
DOI:10.1002/hlca.19850680615
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