Benzoic acid, 4-(2-propenyloxy)-, 4-methoxyphenyl ester

Base Information

Chemical Name:Benzoic acid, 4-(2-propenyloxy)-, 4-methoxyphenyl ester
CAS No.:73376-32-6
Molecular Formula:C17H16O4
Molecular Weight:284.312
Hs Code.:
DSSTox Substance ID:DTXSID90366905
Nikkaji Number:J782.727J
Wikidata:Q82152375

Synonyms:73376-32-6;Benzoic acid, 4-(2-propenyloxy)-, 4-methoxyphenyl ester;4-Allyloxy-benzoic acid 4-methoxy-phenyl ester;Oprea1_720607;Oprea1_800620;SCHEMBL5089928;DTXSID90366905;4-methoxyphenyl-4-allyloxy benzoate;AKOS000618574;4-Allyloxybenzoic acid 4-methoxyphenyl ester

Suppliers and Price of Benzoic acid, 4-(2-propenyloxy)-, 4-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 Benzoic acid, 4-(2-propenyloxy)-, 4-methoxyphenyl ester

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:284.10485899
Heavy Atom Count:21
Complexity:326

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)OC(=O)C2=CC=C(C=C2)OCC=C

Technology Process of Benzoic acid, 4-(2-propenyloxy)-, 4-methoxyphenyl ester

There total 6 articles about Benzoic acid, 4-(2-propenyloxy)-, 4-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: 91.0%

: 27914-60-9
4-allyloxybenzoic acid

: 150-76-5
4-methoxy-phenol

: 73376-32-6
<4-(allyloxy)benzoyloxy>-4-methoxybenzene

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1039/c5tc04331j

Reference yield: 64.0%

: 36844-51-6
4-allyloxybenzoyl chloride

: 150-76-5
4-methoxy-phenol

: 73376-32-6
<4-(allyloxy)benzoyloxy>-4-methoxybenzene

Guidance literature:: With pyridine; In tetrahydrofuran; 1) room temperature, 4 h, 2) 60 deg C, 2 h;
DOI:10.1021/ac00280a019

Reference yield:

: 120-47-8
Ethyl 4-hydroxybenzoate

: 73376-32-6
<4-(allyloxy)benzoyloxy>-4-methoxybenzene

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 10 h / 85 °C / Reflux

2: potassium hydroxide / ethanol; water / 5 h / 105 °C / Reflux

3: dmap; dicyclohexyl-carbodiimide / dichloromethane / 24 h / 20 °C

With dmap; potassium carbonate; dicyclohexyl-carbodiimide; potassium hydroxide; In ethanol; dichloromethane; water; acetonitrile;
DOI:10.1039/c5tc04331j