Docosyl ferulate

Base Information Edit

Chemical Name:Docosyl ferulate
CAS No.:101927-24-6
Molecular Formula:C32H54O4
Molecular Weight:502.778
Hs Code.:2918992090
European Community (EC) Number:888-018-2
UNII:A2T8GNE262
Nikkaji Number:J370.105K,J503.472H
Wikidata:Q27136483
Mol file:101927-24-6.mol

Synonyms:docosyl ferulate;101927-24-6;(E)-Docosyl 3-(4-hydroxy-3-methoxyphenyl)acrylate;Docosyl trans-ferulate;docosyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate;2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, docosyl ester, (2E)-;CHEBI:68000;DOCOSYL FERULATE [USP-RS];BEA92724;G69422;(E)-Docosyl3-(4-hydroxy-3-methoxyphenyl)acrylate;Q27136483;DOCOSYL TRANS-FERULATE (CONSTITUENT OF PYGEUM) [DSC]

Suppliers and Price of Docosyl ferulate

Supply Marketing:Edit

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Docosyl ferulate Edit

Chemical Property:

PSA：55.76000
LogP:9.77910
XLogP3:12.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:25
Exact Mass:502.40221020
Heavy Atom Count:36
Complexity:518

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC
Isomeric SMILES:CCCCCCCCCCCCCCCCCCCCCCOC(=O)/C=C/C1=CC(=C(C=C1)O)OC
Uses Docosyl Ferulate is a compound derived form Ferulic Acid (F308900), widely distributed in small amounts in plants. Used as an antioxidant and food preservative.

Technology Process of Docosyl ferulate

There total 6 articles about Docosyl ferulate 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: 69.0%

: C₃₅H₅₈O₆

: 101927-24-6
(E)-ferulic acid docosyl ester

Guidance literature:: With piperidine; In dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1021/acs.jnatprod.8b01023

Reference yield:

: 91471-08-8
3-methoxy-4-(tetrahydropyran-2-yloxy)benzaldehyde

: 101927-24-6
(E)-ferulic acid docosyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 40 percent / piperidine, aniline / pyridine / 15 h / 70 - 80 °C

2: DCC / pyridine

3: 1M HCl / tetrahydrofuran / 1 h / Ambient temperature

With hydrogenchloride; dicyclohexyl-carbodiimide; piperidine; aniline; In tetrahydrofuran; pyridine;
DOI:10.1016/0031-9422(92)83695-U