Hexyl cinnamate

Base Information

Chemical Name:Hexyl cinnamate
CAS No.:3488-00-4
Molecular Formula:C15H20 O2
Molecular Weight:232.323
Hs Code.:2916399090
European Community (EC) Number:222-479-7
UNII:532UJ0Y6RI
Nikkaji Number:J184.152A,J216.149D
Wikidata:Q20081199
RXCUI:2604566
Mol file:3488-00-4.mol

Synonyms:Hexyl cinnamate;3488-00-4;hexyl (E)-3-phenylprop-2-enoate;532UJ0Y6RI;trans-cinnamic acid hexyl ester;EINECS 222-479-7;2-Propenoic acid, 3-phenyl-, hexyl ester;n-hexyl cinnamate;Cinnamic acid hexyl ester;UNII-532UJ0Y6RI;SCHEMBL1170007;3-Phenylpropenoic acid hexyl ester;CINNAMIC ACID, HEXYL ESTER;Q20081199

Suppliers and Price of Hexyl cinnamate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
HEXYL CINNAMATE 95.00%
5MG
$ 503.49

Total 8 raw suppliers

Chemical Property of Hexyl cinnamate

Chemical Property:

Vapor Pressure:0.000126mmHg at 25°C
Boiling Point:334.7°C at 760 mmHg
Flash Point:179.1°C
PSA：26.30000
Density:0.997g/cm³
LogP:3.82330
XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:232.146329876
Heavy Atom Count:17
Complexity:227

Purity/Quality:

99% ^*data from raw suppliers

HEXYL CINNAMATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCOC(=O)C=CC1=CC=CC=C1
Isomeric SMILES:CCCCCCOC(=O)/C=C/C1=CC=CC=C1

Technology Process of Hexyl cinnamate

There total 16 articles about Hexyl 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: 95.0%

: 140-10-3
(E)-3-phenylacrylic acid

: 111-27-3
hexan-1-ol

: 3488-00-4
n-hexyl cinnamate

Guidance literature:: With glucose-diphenylaminium tosylate-derived carbon solid acid (GDTCSA); In n-heptane; at 80 ℃; for 24h;
DOI:10.1039/c4gc01395f