3'-Acetoxyacetophenone is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry laboratories, where it is employed to facilitate carbon-carbon bond formation and molecular structure modification. This compound is particularly valuable in the development of aromatic and heterocyclic compounds due to its stability and reactivity. Its versatility makes it an essential reagent in various synthetic pathways, contributing to the advancement of chemical research and innovation.
The compound's favorable chemical properties, including its stability and moderate reactivity, make it a preferred choice for laboratory applications. It is capable of participating in multiple reaction mechanisms, such as SN1, SN2, and electrophilic substitution reactions. These characteristics allow it to be used in a wide range of synthetic processes, making it a reliable and adaptable reagent for chemists. Its ability to undergo various chemical transformations enhances its utility in both academic and industrial research settings.
In Indonesian laboratories, 3'-Acetoxyacetophenone is commonly used in scientific research, including drug development, industrial chemical production, and the creation of new materials. Its availability and compatibility with different experimental scales make it a popular choice among researchers. The compound's role in organic synthesis supports the growth of chemical innovation in the region, contributing to both academic and industrial advancements.
Related TCI products
- TCI A1997 13031-43-1 4'-Acetoxyacetophenone
- TCI A1995 7250-94-4 2'-Acetoxyacetophenone
- TCI A0067 2623-33-8 4'-Acetoxyacetanilide
- TCI A1500 13831-31-7 Acetoxyacetyl Chloride
- TCI D2843 6946-10-7 1,3-Diacetoxyacetone
- TCI M2696 1195053-25-8 Methyl (Phenyl 5-Acetoxyacetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate
- Synthesis of complex aromatic compounds for pharmaceutical development due to its ability to form stable carbon-carbon bonds.
- Electrophilic substitution reactions in molecular modification as it provides reactive functional groups for further chemical transformations.
- Development of new industrial chemicals through its role in structural changes and functional group introduction.
- Research in material science for the creation of novel polymers and organic materials due to its reactivity and versatility.
- Organic synthesis experiments in academic settings for teaching and research purposes because of its reliability and availability.
| Brand | TCI |
|---|---|
| CAS number | 2454-35-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per standard chemical supply practices |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from direct sunlight |
3'-Acetoxyacetophenone should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its stability. As a reactive chemical, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. It is important to keep the compound away from incompatible substances to avoid any potential chemical reactions. Proper storage and handling practices help maintain its chemical integrity and ensure safe usage in laboratory environments.
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