4-Allyl-2-methoxyphenyl cinnamate

Base Information

• Chemical Name: 4-Allyl-2-methoxyphenyl cinnamate
• CAS No.: 532-08-1
• Molecular Formula: C19H18 O3
• Molecular Weight: 294.35
• Hs Code.: 2916399090
• European Community (EC) Number: 208-526-4
• NSC Number: 46764
• Nikkaji Number: J135.407H,J729.899D
• Wikidata: Q61082202
• ChEMBL ID: CHEMBL2271265
• Mol file: 532-08-1.mol

Synonyms:4-Allyl-2-methoxyphenyl cinnamate;Cinnamyl eugenol;532-08-1;Eugenol cinnamate;EINECS 208-526-4;Cinnamyleugenol;eugenyl cinnamate;Cinnamic acid, ester with eugenol;SCHEMBL4201037;CHEMBL2271265;NSC46764;NSC 46764;NSC-46764;AKOS024336571;Cinnamic acid, 4-allyl-2-methoxyphenyl ester;Cinnamic acid 2-methoxy-4-(2-propenyl)phenyl ester;Q61082202;(4-allyl-2-methoxy-phenyl) (E)-3-phenylprop-2-enoate;2-Propenoic acid, 2-methoxy-4-(2-propenyl)phenyl ester

Chemical Property of 4-Allyl-2-methoxyphenyl cinnamate

Chemical Property:

• Vapor Pressure: 2.32E-08mmHg at 25°C
• Boiling Point: 452°Cat760mmHg
• Flash Point: 193.7°C
• PSA: 35.53000
• Density: 1.113g/cm³
• LogP: 4.04250
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 294.125594432
• Heavy Atom Count: 22
• Complexity: 382

Purity/Quality:

99% ^*data from raw suppliers

4-ALLYL-2-METHOXYPHENYL CINNAMATE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=CC(=C1)CC=C)OC(=O)C=CC2=CC=CC=C2
• Isomeric SMILES: COC1=C(C=CC(=C1)CC=C)OC(=O)/C=C/C2=CC=CC=C2

Technology Process of 4-Allyl-2-methoxyphenyl cinnamate

There total 7 articles about 4-Allyl-2-methoxyphenyl cinnamate 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: 88.0%

benzaldehyde (100-52-7) + (carbo-4-allyl-2-methoxyphenyloxymethylene)triphenylphosphorane (691860-39-6) → 4-allyl-2-methoxyphenyl cinnamate (532-08-1)

Guidance literature:

In dichloromethane; at 20 ℃;

Reference yield: 50.0%

4-allylguaiacol (97-53-0) + (E)-3-phenylacrylic acid (140-10-3) → 4-allyl-2-methoxyphenyl cinnamate (532-08-1)

Guidance literature:

With dmap; dicyclohexyl-carbodiimide; at 20 ℃; for 16h;

DOI:10.3390/molecules19021394

Reference yield: 13.0%

4-allylguaiacol (97-53-0) + Cinnamic acid (621-82-9) → 4-allyl-2-methoxyphenyl cinnamate (532-08-1)

Guidance literature:

DOI:10.1271/bbb.60.909

upstream raw materials:

4-allylguaiacol

cinnamoyl chloride

Cinnamic acid

benzaldehyde