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Phenyl oleate, also known as phenyl ethyl oleate, is an organic compound with the chemical formula C18H30O2. It is a derivative of oleic acid, an unsaturated fatty acid, and is formed by the esterification of oleic acid with phenol. Phenyl oleate is a colorless to pale yellow liquid with a mild odor and is soluble in organic solvents. It is used in various applications, including as a plasticizer, a lubricant, and a component in the production of certain types of resins and coatings. Due to its unique properties, phenyl oleate can enhance the flexibility and adhesion of materials, making it a valuable chemical in the manufacturing industry.

3839-63-2

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3839-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3839-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3839-63:
(6*3)+(5*8)+(4*3)+(3*9)+(2*6)+(1*3)=112
112 % 10 = 2
So 3839-63-2 is a valid CAS Registry Number.

3839-63-2Downstream Products

3839-63-2Relevant academic research and scientific papers

Base catalyzed sustainable synthesis of phenyl esters from carboxylic acids using diphenyl carbonate

Kreye, Oliver,Meier, Michael A. R.

, p. 53155 - 53160 (2015)

Phenyl esters were obtained in moderate to high yields by reaction of aliphatic and aromatic carboxylic acids with one equivalent of diphenyl carbonate in the presence of catalytic amounts of tertiary amine bases, such as DBU, TBD and DMAP under neat conditions at elevated temperatures (>100°C).

Kinetic Control over CdS Nanocrystal Nucleation Using a Library of Thiocarbonates, Thiocarbamates, and Thioureas

Hamachi, Leslie S.,Jen-La Plante, Ilan,Coryell, Aidan C.,De Roo, Jonathan,Owen, Jonathan S.

, p. 8711 - 8719 (2017/10/30)

We report a family of substituted thiocarbonates, thiocarbamates, and thioureas and their reaction with cadmium oleate at 180-240 °C to form zincblende CdS nanocrystals (d = 2.2-5.9 nm). To monitor the kinetics of CdS formation with UV-vis spectroscopy, t

Effect of solvent and ultrasound on esterification of phenols

Rama,Pasha

, p. 2604 - 2605 (2007/10/03)

Phenols are conveniently acylated by acid chlorides in CH2Cl2 under the influence of ultrasound to give esters in satisfactory yields.

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