4'-Chloro-2'-hydroxyacetophenone is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It plays a crucial role in laboratory settings where the construction of specific molecular structures is required. This compound is particularly valued for its ability to participate in various chemical reactions, including substitution and electrophilic reactions. Its versatility makes it an essential tool for chemists working on the development of new materials and pharmaceuticals.
The reactivity of 4'-chloro-2'-hydroxyacetophenone, combined with its capacity to form bonds with different functional groups, makes it a preferred choice in synthetic chemistry. It is stable under normal laboratory conditions, which simplifies its handling and storage. This stability ensures that the compound remains effective for extended periods, allowing researchers to conduct experiments with confidence. Its chemical properties make it suitable for a wide range of applications in both academic and industrial research environments.
In Indonesian laboratories, 4'-chloro-2'-hydroxyacetophenone is extensively used in organic chemistry research, particularly in the fields of pharmaceuticals, materials science, and analytical chemistry. It is commonly employed in experiments that require the modification of molecular structures through chloro and hydroxyl substitutions. Many research institutions and universities rely on this compound for its reliability and effectiveness in complex synthetic processes.
Related TCI products
- TCI C3076 2892-29-7 3'-Chloro-4'-hydroxyacetophenone
- TCI B5382 30186-18-6 4'-Bromo-2'-hydroxyacetophenone
- TCI B5158 1836-06-2 3'-Bromo-4'-hydroxyacetophenone
- TCI B4735 2491-36-3 2-Bromo-2'-hydroxyacetophenone
- TCI B4115 2491-38-5 2-Bromo-4'-hydroxyacetophenone
- TCI A3049 54255-50-4 3'-Amino-4'-hydroxyacetophenone
- Synthesis of pharmacological compounds requiring chloro and hydroxyl substitutions due to its reactive functional groups and structural versatility.
- Electrophilic reactions for building complex molecular structures because of its ability to participate in substitution and functional group transformations.
- Organic material development where precise molecular modifications are essential for creating new polymers and chemical compounds.
- Analytical chemistry experiments that require the use of well-defined building blocks for compound identification and structural analysis.
- Pharmaceutical research applications where the compound is used as an intermediate in drug synthesis and compound modification processes.
| Brand | TCI |
|---|---|
| CAS number | 6921-66-0 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply specifications |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from direct sunlight and incompatible substances |
4'-Chloro-2'-hydroxyacetophenone 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 moisture absorption and contamination. The compound is generally stable under normal laboratory conditions, but it should be handled with care to avoid exposure to incompatible chemicals. Proper labeling and storage in a designated chemical storage area are essential for safety. Laboratory personnel should wear appropriate personal protective equipment when handling this compound to ensure safe usage and minimize potential risks.
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3'-Chloro-4'-hydroxyacetophenone TCI C3076
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