36588-29-1 Usage
Description
(Octadecyloxy)benzene is a chemical compound consisting of a benzene ring with an attached octadecyloxy group, which is an 18-carbon chain. This structure endows the compound with unique properties, allowing it to interact with both water and oil-based substances due to its nonpolar nature.
Uses
Used in Surfactant and Dispersing Agent Applications:
(Octadecyloxy)benzene is used as a surfactant and dispersing agent in various manufacturing processes. Its ability to interact with both water and oil-based substances makes it an effective component for stabilizing mixtures and improving the solubility of various compounds.
Used in Chemical Production:
(Octadecyloxy)benzene serves as an intermediate in the production of other chemicals, such as detergents and emulsifiers. Its versatile structure and properties make it a valuable component in the creation of a wide range of industrial and commercial products.
Used in Pharmaceutical Industry:
(Octadecyloxy)benzene can be used as a component in the formulation of drug delivery systems, potentially enhancing the bioavailability and efficacy of certain medications.
Used in Cosmetics Industry:
In the cosmetics industry, (octadecyloxy)benzene may be utilized as an ingredient in the development of creams, lotions, and other skincare products, where its surfactant properties can improve the texture and stability of the formulations.
Used in Food Industry:
(Octadecyloxy)benzene could also find applications in the food industry as an additive to improve the emulsification properties of certain products, such as sauces, dressings, and spreads.
Check Digit Verification of cas no
The CAS Registry Mumber 36588-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,8 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36588-29:
(7*3)+(6*6)+(5*5)+(4*8)+(3*8)+(2*2)+(1*9)=151
151 % 10 = 1
So 36588-29-1 is a valid CAS Registry Number.
36588-29-1Relevant articles and documents
The Chemistry of Pentavalent Organobismuth Reagents. Part 8. Phenylation and Oxidation of Alcohols by Tetraphenylbismuth Esters
Barton, Derek H. R.,Finet, Jean-Pierre,Motherwell, William B.,Pichon, Clotilde
, p. 251 - 260 (2007/10/02)
Tetraphenylbismuth trifluoroacetate under neutral or slightly acidic conditions O-phenylates primary alcohols in reasonable (65-75percent) yield, but gives only moderate yields with secondary alcohols and no O-phenylation with tertiary alcohols.An SN2 type mechanism is proposed with attack of oxygen on aryl carbon.In contrast, the reaction of Bi(V) reagents with alcohols under basic conditions gives, exclusively, oxidation, often with benzene as a leaving group.The presence of a Bi(V) intermediate with a bismuth-oxygen bond has been proved in several different ways using n.m.r. spectroscopy.Thus the reactions of alcohols with Bi(V) reagents parallel the corresponding reactions with phenols.
