5471-50-1

Usage

Uses

Used in Chemical Synthesis:
3,7-dimethyloct-6-enyl 2-chloroacetate serves as a chemical intermediate, playing a crucial role in the synthesis of a variety of organic and pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the creation of complex molecules for different applications.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, 3,7-dimethyloct-6-enyl 2-chloroacetate is utilized for its distinctive scent and flavor profile. It contributes to the development of new and innovative fragrances and flavorings, enhancing the sensory experience of various consumer products.
Used in Pharmaceutical Industry:
3,7-dimethyloct-6-enyl 2-chloroacetate is also employed in the pharmaceutical sector, where it is used as a precursor in the production of specific drugs. Its reactivity and structural features make it suitable for the synthesis of medicinal compounds, potentially leading to the development of new treatments and therapies.

InChI:InChI=1/C12H21ClO2/c1-10(2)5-4-6-11(3)7-8-15-12(14)9-13/h5,11H,4,6-9H2,1-3H3

Upstream product

• 106-22-9 Citronellol 
• 79-11-8 chloroacetic acid 

Relevant academic research and scientific papers

Novel N-4-Piperazinyl Ciprofloxacin-Ester Hybrids: Synthesis, Biological Evaluation, and Molecular Docking Studies

Abstract: A series of novel N-4-piperazinylciprofloxacin-ester hybrids has been synthesized and the structures confirmed by1H and 13C NMR, FT-IRspectral data, and elemental analysis. The products have been tested in vitro for their antibacterial activity againstsix bacterial strains (MRSA, Staphylococcusepidermidis, Bacillussubtilis, Escherichia coli,Salmonella enterica, and Klebsiella pneumoniae) and have demonstrated goodantibacterial activity with MIC values range 6.25–200 μg/mL. Antifungal andcytotoxic activities of the products have been tested against Candida kefyr and human leukemia K562 cell line,respectively. All compounds inhibit growth of K562 cells more efficiently thanthe parent ciprofoxacin in a dose- and duration-dependent way. Molecular dockingstudies performed for the compound 3i indicatesthat similarly to ciprofloxacin it can act as an inhibitor of S. aureus DNA gyrase.

WATER- OR ACID-TRIGGERED FRAGRANCE RELEASE FUNCTIONAL MONOMER AND POLYMER SYSTEM

A triggerable composition for one-stage, controlled release of a functional chemical includes a functional monomer having a structure selected from the group described herein, wherein R is a polymerizable portion, N+X- is a quaternar

Fragrance alcohol-releasing polysiloxane

Organopolysiloxanes which contain a fragrance alcohol Y—OH bonded via a betaine ester group having the structure —N+R1R2—CH2—C(O)OY, cleave off the fragrance alcohol under acid conditions and are resistant to hydrolysis in the neutral and weakly basic range. The organopolysiloxanes adhere to textile fibres, skin or hair and are suitable as perfume components for textile treatment agents and personal care products.