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2-(4-Methoxyphenyl)butanal

Base Information
  • Chemical Name:2-(4-Methoxyphenyl)butanal
  • CAS No.:50838-58-9
  • Molecular Formula:C11H14O2
  • Molecular Weight:178.231
  • Hs Code.:
  • European Community (EC) Number:836-928-5
  • Nikkaji Number:J788.061H
2-(4-Methoxyphenyl)butanal

Synonyms:2-(4-methoxyphenyl)butanal;50838-58-9;SCHEMBL5789571;AKOS014312356;G50109;EN300-7352682;Z1255400148

Suppliers and Price of 2-(4-Methoxyphenyl)butanal
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-(4-Methoxyphenyl)butanal
Chemical Property:
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:178.099379685
  • Heavy Atom Count:13
  • Complexity:148
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(C=O)C1=CC=C(C=C1)OC
Technology Process of 2-(4-Methoxyphenyl)butanal

There total 11 articles about 2-(4-Methoxyphenyl)butanal 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-iodo-succinimide; water; cetyltrimethylammonim bromide; In 1,4-dioxane; at 20 - 105 ℃; for 0.333333h; Microwave irradiation;
DOI:10.1039/b908717f
Guidance literature:
With methoxy(cyclooctadiene)rhodium(I) dimer; trisodium tris(3-sulfophenyl)phosphine; hydrogen; cetyltrimethylammonim bromide; In water; at 100 ℃; for 1h; under 15001.5 Torr; regioselective reaction; Autoclave; Schlenk technique; Inert atmosphere;
DOI:10.1016/j.apcata.2014.11.028
Guidance literature:
With methoxy(cyclooctadiene)rhodium(I) dimer; tri(o-t-butylphenyl)phosphite; hydrogen; In toluene; at 80 ℃; for 24h; under 30003 Torr; Reagent/catalyst; regioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.apcata.2015.02.028
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