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4-PENTYN-1-OL

Base Information Edit
  • Chemical Name:4-PENTYN-1-OL
  • CAS No.:390-04-5
  • Molecular Formula:C15H11 F O3
  • Molecular Weight:258.249
  • Hs Code.:2918300090
  • Mol file:390-04-5.mol
4-PENTYN-1-OL

Synonyms:Benzoicacid, o-(2-fluoro-p-toluoyl)- (8CI); Benzophenone,2'-fluoro-4'-methyl-2-carboxy-

Suppliers and Price of 4-PENTYN-1-OL
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
Total 3 raw suppliers
Chemical Property of 4-PENTYN-1-OL Edit
Chemical Property:
  • PSA:20.23000 
  • LogP:0.39210 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-PENTYN-1-OL

There total 1 articles about 4-PENTYN-1-OL 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;
upstream raw materials:

phthalic anhydride

m-Fluorotoluene

Refernces Edit

SYNTHESIS OF COMPLEX PYRIDINE BASES IN THE REACTION OF α,ω-NITRILEACETYLENES WITH ACETYLENE, CATALYZED BY COBALT COMPLEXES

10.1007/BF00954829

The research focuses on the synthesis of complex pyridine bases through the reaction of α,ω-nitrileacetylenes with acetylene, catalyzed by cobalt complexes. The study investigates the reactivity of various α,ω-nitrileacetylenes, including those containing an oxygen atom, in the oligomerization reaction with acetylene. Key chemicals involved include α,ω-nitrileacetylenes such as propargyl alcohol, 4-pentyn-1-ol, acrylonitrile, and 6-bromohex-1-yne, as well as the cobalt catalyst Co(2-ethyl hexanoate)2 and AlEt3. The research explores the cyclocodimerization process in a toluene solution at 150°C and under an acetylene pressure of 10-15 atm, leading to the formation of various pyridine derivatives and benzene products. The study also examines the effects of different nitrile/acetylene ratios on product yields and the reactivity differences between oxygen-containing nitrileacetylenes and simpler nitroacetylenes.

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