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pentan-3-yl prop-2-enoate

Base Information
  • Chemical Name:pentan-3-yl prop-2-enoate
  • CAS No.:4513-35-3
  • Molecular Formula:C8H14O2
  • Molecular Weight:142.198
  • Hs Code.:
pentan-3-yl prop-2-enoate

Synonyms:

Suppliers and Price of pentan-3-yl prop-2-enoate
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
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  • price
Total 1 raw suppliers
Chemical Property of pentan-3-yl prop-2-enoate
Chemical Property:
  • Vapor Pressure:2.079mmHg at 25°C 
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of pentan-3-yl prop-2-enoate

There total 1 articles about pentan-3-yl prop-2-enoate 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 n-butyllithium; bis(acetylacetonate)nickel(II); In benzene; at 90 ℃; for 5h; Product distribution; other temp., other time;
Guidance literature:
Multi-step reaction with 2 steps
1: 72 percent / 1,4-diazabicyclo<2.2.2>octane (DABO) / 4 h / 50 °C / 3750300 Torr
2: 15 percent Chromat. / Cp2ZrCl2, NaAlH2(OCH2CH2OMe)2 / tetrahydrofuran; toluene / 1 h / -78 °C
With 1,4-diaza-bicyclo[2.2.2]octane; zirconocene dichloride; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; toluene;
DOI:10.1007/BF00960333
Guidance literature:
Multi-step reaction with 4 steps
1: 44 percent / DABCO / acetonitrile / 192 h / sonicated
2: 78 percent / imidazole / dimethylformamide / 16 h / 20 °C
3: H2 / 5 percent Pd/C / ethyl acetate / 16 h / 20 °C
4: 80 percent / 48 percent HF / acetonitrile / 1 h / 20 °C
With 1,4-diaza-bicyclo[2.2.2]octane; 1H-imidazole; hydrogen fluoride; hydrogen; palladium on activated charcoal; In ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 1: Baylis-Hillman reaction;
DOI:10.1016/S0040-4020(01)00647-0
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