50433-83-5

Usage

Uses

Used in Fragrance and Flavor Industry:
(4-formylphenyl) octanoate is used as a key ingredient for creating fragrances and flavors due to its appealing and fruity scent. It adds a unique and refreshing aroma to a wide range of products, enhancing their overall sensory experience.
Used in Cosmetics and Personal Care Industry:
In the cosmetics and personal care sector, (4-formylphenyl) octanoate serves as an essential component in the formulation of various products. Its pleasant odor and compatibility with other ingredients make it a popular choice for enhancing the fragrance and improving the overall quality of these products.
Used in Pharmaceutical Industry:
(4-formylphenyl) octanoate is employed as a reagent in the pharmaceutical industry, where it plays a crucial role in the development and production of various medications. Its unique chemical properties allow it to be used in the synthesis of different drug compounds, contributing to the advancement of medical treatments.
Used in Chemical Research:
As a valuable compound in chemical research, (4-formylphenyl) octanoate is utilized for various experimental purposes. Its distinctive properties make it an ideal candidate for studying chemical reactions and exploring new applications in the field of chemistry.

InChI:InChI=1/C15H20O3/c1-2-3-4-5-6-7-15(17)18-14-10-8-13(12-16)9-11-14/h8-12H,2-7H2,1H3

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 111-64-8 n-octanoic acid chloride 
• 124-07-2 Octanoic acid 

Downstream Products

• 56670-31-6 4-octanoyloxybenzoic acid 
• 134293-39-3 4,4'-bis(4-heptylcarbonyloxybenzylideneamino)stilbene 
• 134293-36-0 4,4'-bis(4-heptylcarbonyloxybenzylideneamino)azobenzene 

Relevant academic research and scientific papers

BISPHOSPHONATE COMPOUNDS

Novel bisphosphonate cyclic acetal compounds are disclosed, as well as methods of preparing the compounds, pharmaceutical compositions including the compounds, and administration of the compounds in methods of treating bone metabolism disorders, such as abnormal calcium and phosphate metabolism.

Liquid Crystalline Azomethines and Polyazomethines Containing Azobenzene and Stilben Units

Azobenzene and stilbene derivatives with azomethine and ester groups and polymers of corresponding structures with mesogens possessing three to four aromatic systems in their mesogenic units have been synthesized, characterized and studied for their liquid crystalline properties by DSC measurements and observation by polarizing microscopy.

Liquid-crystalline substituted biphenyl esters

Novel ferroelectric liquid crystals exhibiting a chiral smectic C phase and liquid crystal compositions containing the same are provided, which liquid crystals are substituted biphenyl esters expressed by the general formula STR1 wherein R1 * represents an optically active alkyl group of 4 to 18 carbon atoms; STR2 represents STR3 or STR4 Z represents R2, R2 CO or R2 COO wherein R2 represents an alkyl group or an alkoxy group each of 1 to 18 carbon atoms; and X and Y each represent hydrogen atom (H), bromine atom (Br), chlorine atom (Cl), fluorine atom (F) or cyano group (CN), and either one of X or Y is always hydrogen atom.

The Effect of Carbonyl Containing Substituents in the Terminal Chains on Mesomorphic Properties in Some Aromatic Esters and Thioesters. 3. Acyloxy Groups on the Acid End

A select number of 4-alkyl and alkoxyphenyl-4'-acyloxybenzoates and phenylthiobenzoates of the type where X = RCO2, Y = R' or OR', and Z = O or S have been prepared and their mesomorphic properties determined by hot-stage polarizing microscopy.T