Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 4-5 minggu setelah pembayaran.
Couldn't load pickup availability
Description
2-Chloro-4-nitrobenzamide is a versatile organic compound widely used in laboratory settings for its reactivity and utility in synthetic chemistry. As a building block in organic synthesis, it plays a critical role in the development of complex molecules through various chemical reactions. Its presence in chemical laboratories makes it an essential tool for researchers and students alike. This compound is commonly employed in both academic and industrial research to facilitate the creation of new chemical entities with tailored properties.
The compound’s unique electronic properties, derived from the presence of both chloro and nitro groups, make it a preferred choice in synthetic pathways. These substituents influence the molecule’s reactivity, enabling it to participate in electrophilic and nucleophilic substitution reactions. Its stability under controlled reaction conditions further enhances its reliability in laboratory applications. The ability to modify its structure through chemical transformations also makes it a valuable asset in the field of medicinal and materials chemistry.
In Indonesian laboratories, 2-Chloro-4-nitrobenzamide is frequently used in organic chemistry research, particularly in educational and advanced research settings. Its availability and reliability make it a go-to compound for both teaching and experimental purposes. Its role in coupling reactions, acylation, and substitution processes ensures its continued relevance in the chemical research landscape of Indonesia.
Laboratory Applications
Organic synthesis applications benefit from its reactivity and versatility in creating complex molecules through various chemical reactions.
It is ideal for coupling reactions due to its ability to form stable intermediates and participate in bond-forming processes.
In acylation reactions, it serves as a valuable acylating agent, enabling the introduction of acyl groups into organic molecules.
Its use in substitution reactions is widespread, as the chloro and nitro groups provide unique electronic effects that influence reaction pathways.
Educational laboratories rely on it for teaching fundamental concepts in organic chemistry and synthetic methodologies.
Specifications
Brand: TCI
CAS number: 3011-89-0
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes: Available in standard laboratory quantities
Physical form: Solid
Storage note: Store in a cool, dry place away from light and moisture
Handling and Storage
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to humidity and potential degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. While it is generally stable under normal storage conditions, it should be kept away from incompatible substances to avoid any unwanted chemical interactions. Proper labeling and storage practices are essential to maintain the integrity of the compound and ensure safe handling in laboratory settings.
