Octyl 4-methoxycinnamate

Basic information

  • Product Name:Octyl 4-methoxycinnamate
  • CasNo.:5466-77-3
  • MF:C18H26O3

Physical and Chemical Properties

  • Purity:99%
  • Melting Point:<-25℃
  • Appearance:colourless or pale yellow liquid
Inquiry

Product Details

CasNo: 5466-77-3

MF: C18H26O3

Appearance: colourless or pale yellow liquid

Quality Factory Sells Top Purity 99% Octyl 4-methoxycinnamate 5466-77-3 with Safe Delivery

  • Molecular Formula:C18H26O3
  • Molecular Weight:290.403
  • Appearance/Colour:colourless or pale yellow liquid 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:<-25℃ 
  • Refractive Index:1.543-1.547 
  • Boiling Point:405.3 °C at 760 mmHg 
  • Flash Point:171.6 °C 
  • PSA:35.53000 
  • Density:1 g/cm3 
  • LogP:4.46800 

Octyl 4-methoxycinnamate(Cas 5466-77-3) Usage

Octyl 4-methoxycinnamate is a colorless to light yellow oily liquid. It is a common UV absorber and is widely used in cosmetics and sunscreen products. Octyl 4-methoxycinnamate can effectively absorb UVA radiation, reduce UV damage to the skin, and prevent skin tanning and sunburn. It is usually prepared by chemical synthesis. In the field of cosmetics, it is an important ingredient in many sunscreens, lotions and creams. For example, in summer outdoor activities, using sunscreen products containing octyl 4-methoxycinnamate can reduce the risk of skin damage by UV rays and keep the skin healthy.

InChI:InChI=1/C18H26O3/c1-4-6-7-8-16(5-2)21-18(19)14-11-15-9-12-17(20-3)13-10-15/h9-14,16H,4-8H2,1-3H3/b14-11+

5466-77-3 Relevant articles

Cross metathesis with acrylates: N-heterocyclic carbene (NHC)- versus cyclic alkyl amino carbene (CAAC)-based ruthenium catalysts, an unanticipated influence of the carbene type on efficiency and selectivity of the reaction

Kaczanowska, Katarzyna,Trzaskowski, Bartosz,Peszczyńska, Aleksandra,Tracz, Andrzej,Gawin, Rafa?,Olszewski, Tomasz K.,Skowerski, Krzysztof

, p. 6366 - 6374 (2020)

Olefin metathesis has been widely explor...

Aquatic Fate of Sunscreen Agents Octyl-4-methoxycinnamate and Octyl-4-dimethylaminobenzoate in Model Swimming Pools and the Mutagenic Assays of Their Chlorination Byproducts

Mariko Nakajima, Tsuyoshi Kawakami, Tatsuhiro Niino, Yasuo Takahashi, Sukeo Onodera

Journal of Health Science

Reactions of sunscreen agents, octyl dimethyl-p-aminobenzoate (ODPABA) and octyl-p-methoxycinnamate (OMC), with hypochlorite in aqueous solution were investigated under the conditions that simulate swimming pool disinfection sites.

Palladium-Based Catalysts Supported by Unsymmetrical XYC–1 Type Pincer Ligands: C5 Arylation of Imidazoles and Synthesis of Octinoxate Utilizing the Mizoroki–Heck Reaction

Maji, Ankur,Singh, Ovender,Singh, Sain,Mohanty, Aurobinda,Maji, Pradip K.,Ghosh, Kaushik

, p. 1596 - 1611 (2020/04/29)

A series of new unsymmetrical (XYC–1 typ...

Mimics of Pincer Ligands: An Accessible Phosphine-Free N-(Pyrimidin-2-yl)-1,2-azole-3-carboxamide Framework for Binuclear Pd(II) Complexes and High-Turnover Catalysis in Water

Bumagin, Nikolay A.,Dikusar, Evgenij A.,Ivashkevich, Ludmila S.,Kletskov, Alexey V.,Kolesnik, Iryna A.,Lyakhov, Alexander S.,Petkevich, Sergey K.,Potkin, Vladimir I.

supporting information, (2020/08/12)

We report for the first time cyclic phos...

5466-77-3 Process route

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-iodoanisole
696-62-8

para-iodoanisole

2-ethylhexyl methoxycinnamate
5466-77-3,83834-59-7

2-ethylhexyl methoxycinnamate

Conditions
Conditions Yield
With tetrabutylammomium bromide; C32H26Cl2N8O4Pd2; potassium carbonate; In methanol; water; for 0.416667h; Reflux;
97%
With C43H54NO5P; palladium diacetate; triethylamine; In water; at 40 ℃; for 12h;
95%
With tributyl-amine; chloro-[2-(9-phenyl-1,10-phenanthrolin-2-yl)phenyl]palladium; In 1-methyl-pyrrolidin-2-one; at 140 ℃; for 15h; Inert atmosphere;
94%
With (Bis(tri-tert-butylphosphine)palladium(0)); SPGS-550-M; NOK; triethylamine; In water; for 5h; Reagent/catalyst; Inert atmosphere; Microwave irradiation; Sealed tube;
93%
With triethylamine; 4,4'-dichlorobenzophenone oxime derived palladacycle; In 1-methyl-pyrrolidin-2-one; at 110 ℃; for 22h;
85%
With dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); pyridinium p-toluenesulfonate; triethylamine; In water; at 20 ℃; under 760.051 Torr; Inert atmosphere; Micellar solution;
84%
With 1-methyl-pyrrolidin-2-one; triethylamine; polymer-bound Pd(0) phosphine catalyst; at 90 ℃;
 
With acetic acid; diisopropylamine; palladium on charcoal; In toluene;
 
With potassium acetate; In 1-methyl-pyrrolidin-2-one; at 135 ℃; for 24h;
60 %Chromat.
1-bromo-4-methoxy-benzene
104-92-7

1-bromo-4-methoxy-benzene

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl methoxycinnamate
5466-77-3,83834-59-7

2-ethylhexyl methoxycinnamate

Conditions
Conditions Yield
With tris(dibenzylideneacetone)dipalladium (0); tri-tert-butyl phosphine; Cy2NMe2; In 1,4-dioxane; at 20 ℃; for 148h;
83%
With C21H21ClN4Pd; triethylamine; In 1-methyl-pyrrolidin-2-one; at 140 ℃; for 8h;
73%
With sodium acetate; *6Ph4PCl; In various solvent(s); at 130 ℃;
71%
With tri-n-propylamine; In 1-methyl-pyrrolidin-2-one; at 175 ℃; for 24h; Inert atmosphere;
34%
With dimethylaminoacetic acid; bis(benzonitrile)palladium(II) dichloride;
 

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