53596-82-0

Usage

Uses

Used in the Food Industry:
1-Nonanol, 9-bromo-, acetate is used as a flavoring agent for its ability to impart specific tastes and aromas to food products. Its unique chemical structure allows it to enhance the sensory experience of consumers, making it a valuable ingredient in the creation of various food items.
Used in Fragrance and Perfume Production:
In the fragrance and perfume industry, 1-Nonanol, 9-bromo-, acetate serves as a raw material due to its distinctive scent profile. It contributes to the development of complex and long-lasting fragrances, adding depth and character to perfume compositions.
Used as an Industrial Solvent:
This ester is utilized as a solvent in various industrial processes, where its high boiling point and stability as a liquid are advantageous. It can dissolve a wide range of substances, making it suitable for applications in chemical manufacturing and other industries that require stable solvents.
Used in Organic Synthesis:
1-Nonanol, 9-bromo-, acetate may have potential applications in the field of organic synthesis, where it can act as a starting material or an intermediate in the production of more complex organic compounds. Its unique structure and reactivity can be harnessed to create a variety of chemical products.
Used in Catalyst Development:
1-Nonanol, 9-bromo-, acetate may also find use in the development of catalysts, where its unique properties can be employed to facilitate specific chemical reactions. Its presence can enhance the efficiency and selectivity of catalytic processes, contributing to advancements in chemical research and industrial applications.

Upstream product

• 4549-33-1 1,9-Dibromononane 
• 127-08-2 potassium acetate 
• 55362-80-6 9-bromononan-1-ol 
• 108-24-7 acetic anhydride 

Downstream Products

• 13038-21-6 non-8-en-1-ol 
• 55362-79-3 (9-Acetoxynonyl)-triphenylphosphonium-bromid 
• 13038-22-7 non-8-en-1-yl acetate 
• 180782-78-9 1-(hydroxycarbonyl)pentadec-10(S)-yl O-(4,6-O-benzylidene-β-D-glucopyranosyl)-(1->2)-3,4-O-isopropylidene-β-D-fucopyranoside 
• 180782-75-6 1-(methoxycarbonyl)pentadec-10(S)-yl O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->2)-3,4-O-isopropylidene-β-D-fucopyranoside 
• 180782-81-4 (S)-1-(hydroxycarbonyl)pentadec-10-yl O-(4,6-O-benzylidene-β-D-glucopyranosyl)-(1->2)-3,4-O-isopropylidene-β-D-fucopyranoside 1,3-(B)-lactone 
• 55362-82-8 Acetic acid 8-(5,5,6,6-tetracyano-4-ethyl-cyclohex-2-enyl)-octyl ester 
• 807639-50-5 1-nonanol,9-(4-chloro-2-nitrophenoxy)-,acetate(ester) 
• 77712-29-9 6-(10-hydroxydecyl)-2,3-dimethoxy-5-methylphenol 
• 104967-07-9 2-(10-acetoxy-1-oxodecyl)-3,4,5-trimethoxytoluene 
• 104966-92-9 Acetic acid 10-(2-hydroxy-3,4-dimethoxy-6-methyl-phenyl)-10-oxo-decyl ester 
• 77712-30-2 6-(10-acetoxydecyl)-2,3-dimethoxy-5-methylphenol 
• 104967-08-0 6-(10-acetoxy-1-oxodecyl)-3-hydroxy-2-methoxy-5-methylphenol 
• 104967-09-1 6-(10-acetoxy-1-oxodecyl)-2-hydroxy-3-methoxy-5-methylphenol 

Relevant academic research and scientific papers

Facile synthesis of 3-(ω-acetoxyalkyl)thiophenes and derived copolythiophenes using Rieke zinc

An optimized synthetic protocol toward highly reactive Rieke zinc is applied for the preparation of a series of ω-(2,5-dibromothiophene-3-yl) alkyl acetate monomers and statistical copolythiophenes derived thereof, with 10% of ester-functionalized side chains. The obtained conjugated polymers are attractive electron donor materials for organic solar cells, notably to increase the thermodynamic stability of the bulk heterojunction polymer:fullerene active layer blend, and are fully characterized by a combination of spectroscopic, thermal analysis and electrochemical techniques.

REDOX MOLECULES AND METHODS OF MAKING THE SAME

A non-leaching mediator may include a compound or a mixture of compounds that is not substantially released into a biological sample, but that may be oxidized or reduced, and may transfer one or more electrons from the sample to an electrode of a biosensor. Compounds having the general formulas (I), (II) and/or (III), and/or mixtures or derivatives of these compounds, may be useful as mediators having little or no ability to leach into a sample.

Zn(ClO4)2·6H2O as a Powerful Catalyst for a Practical Acylation of Alcohols with Acid Anhydrides

A new protocol for the acylation of alcohols with anhydrides in the presence of Zn(ClO4)2·6H2O as the catalyst is reported. The activity of Zn(ClO4)2· 6H2O has been proven to be superior to that exerted by dry Mg(ClO4)2 and by metal triflates. Its efficiency allows reactions between poorly reactive substrates, such as sterically hindered tertiary alcohols and aromatic anhydrides, All of the reactions were carried out at a 1:1.05 alcohol/anhydride ratio. These conditions are extremely convenient from a practical and economic point of view, since they avoid wasting reagents and allow a simple workup procedure. The catalytic action of Zn(ClO4)2·6H2O is so specific for the activation of the anhydrides, that acid-sensitive functionalities and the stereochemical configuration of the starting materials remain unaltered in the esterification process. In all cases, the acylated products are quantitatively obtained in pure form. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

Mg(ClO4)2 as a powerful catalyst for the acylation of alcohols under solvent-free conditions

A trace amount of magnesium perchlorate (from 0.1 mol% to 1 mol%) is able to promote quantitative acylation, with anhydrides, of a large variety of functionalized alcohols in short times, at room temperature and under solvent-free conditions.