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2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER

Base Information
  • Chemical Name:2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER
  • CAS No.:66313-10-8
  • Molecular Formula:C8H12O3
  • Molecular Weight:156.181
  • Hs Code.:
2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER

Synonyms:2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER;

Suppliers and Price of 2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER 95.00%
  • 5MG
  • $ 495.98
Total 2 raw suppliers
Chemical Property of 2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER
Chemical Property:
  • Vapor Pressure:0.242mmHg at 25°C 
  • Boiling Point:206oC at 760 mmHg 
  • Flash Point:77.5oC 
  • PSA:35.53000 
  • Density:1.01g/cm3 
  • LogP:0.58780 
Purity/Quality:

99% *data from raw suppliers

2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-METHOXY-PENT-4-YNOIC ACID ETHYL ESTER

There total 2 articles about 2-METHOXY-PENT-4-YNOIC ACID 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 sodium hydride; In tetrahydrofuran;
DOI:10.1021/jo050400a
Guidance literature:
Multi-step reaction with 5 steps
1.1: LiAlH4 / tetrahydrofuran
2.1: 61 percent / oxalyl chloride; DMSO; triethylamine / CH2Cl2 / -70 - 20 °C
3.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
3.2: 58 percent / tetrahydrofuran; hexane / -78 - 20 °C
4.1: triethylamine / PdCl2(PPh3)2; CuI / 5 h / 80 °C
5.1: 304 mg / n-Bu4NF / tetrahydrofuran / 2.5 h / 20 °C
With lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; tetrabutyl ammonium fluoride; dimethyl sulfoxide; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; hexane; dichloromethane; 2.1: Swern oxidation / 4.1: Sonogashira reaction;
DOI:10.1021/jo050400a
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