Octanoic acid, 4-formyl-2-methoxyphenyl ester

Base Information

Chemical Name:Octanoic acid, 4-formyl-2-methoxyphenyl ester
CAS No.:765298-70-2
Molecular Formula:C16H22O4
Molecular Weight:278.348
Hs Code.:
DSSTox Substance ID:DTXSID50477622
Wikidata:Q82310424

Synonyms:Octanoic acid, 4-formyl-2-methoxyphenyl ester;765298-70-2;DTXSID50477622

Suppliers and Price of Octanoic acid, 4-formyl-2-methoxyphenyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Octanoic acid, 4-formyl-2-methoxyphenyl ester

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:278.15180918
Heavy Atom Count:20
Complexity:290

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC(=O)OC1=C(C=C(C=C1)C=O)OC

Technology Process of Octanoic acid, 4-formyl-2-methoxyphenyl ester

There total 2 articles about Octanoic acid, 4-formyl-2-methoxyphenyl 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:

Reference yield: 77.0%

: 121-33-5,8014-42-4
vanillin

: 111-64-8
n-octanoic acid chloride

: 765298-70-2
octanoic acid 4-formyl-2-methoxy-phenyl ester

Guidance literature:: With pyridine; In dichloromethane; for 1h; Heating;
DOI:10.1023/B:RUJO.0000043718.23826.ac DOI:10.1023/B:CONC.0000025473.93772.9e DOI:10.1007/s11167-005-0242-y

Reference yield:

: 124-07-2
Octanoic acid

: 765298-70-2
octanoic acid 4-formyl-2-methoxy-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / benzene / Heating

2: 77 percent / pyridine / CH₂Cl₂ / 1 h / Heating

With pyridine; thionyl chloride; In dichloromethane; benzene;
DOI:10.1007/s11167-005-0242-y