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2-Pentenoic acid, 3,4-dimethyl-, ethyl ester

Base Information Edit
  • Chemical Name:2-Pentenoic acid, 3,4-dimethyl-, ethyl ester
  • CAS No.:6570-79-2
  • Molecular Formula:C9H16O2
  • Molecular Weight:156.225
  • Hs Code.:
  • Mol file:6570-79-2.mol
2-Pentenoic acid, 3,4-dimethyl-, ethyl ester

Synonyms:

Suppliers and Price of 2-Pentenoic acid, 3,4-dimethyl-, ethyl ester
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 2-Pentenoic acid, 3,4-dimethyl-, ethyl ester Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-Pentenoic acid, 3,4-dimethyl-, ethyl ester

There total 1 articles about 2-Pentenoic acid, 3,4-dimethyl-, ethyl ester 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 1,2-dimethyl-1H-imidazole; In diethyl ether; at 51 ℃; Quantum yield; Product distribution; Mechanism; Irradiation; with 3,4-dimethyl derivatives, other products; other solvents, without base;
DOI:10.1139/v84-332
Guidance literature:
Multi-step reaction with 2 steps
1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -78 °C
2: phosphorus tribromide / dichloromethane / 1 h / 0 °C
With phosphorus tribromide; diisobutylaluminium hydride; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1039/c5ob00594a
Guidance literature:
Multi-step reaction with 3 steps
1.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -78 °C
2.1: phosphorus tribromide / dichloromethane / 1 h / 0 °C
3.1: isopropylmagnesium chloride; lithium chloride / tetrahydrofuran / 3 h / -30 °C / Inert atmosphere; Schlenk technique
3.2: 24 h / -40 °C / Inert atmosphere; Schlenk technique
With isopropylmagnesium chloride; phosphorus tribromide; diisobutylaluminium hydride; lithium chloride; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1039/c5ob00594a
upstream raw materials:

ethyl 3,4,4-trimethylpent-2-enoate

Downstream raw materials:

prenyl bromide

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