bicalulutamide
90357-53-2
White to beige powder
Loss on drying ≤ 0.5%
Solution color ≤ BY4
Purity ≥ 98.5%, maximum single unknown impurity ≤ 0.2%, total impurities ≤ 1.5%
Availability: | |
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Product Description
We are a pharmaceutical intermediate manufacturer of N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methacrylamide.
Its CAS No. is 90357-53-2
Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, etc.
Product Category | Bicalutamide |
CAS NO | 90357-53-2 |
Product Specifications | White to beige powder Loss on drying ≤ 0.5% Solution color ≤ BY4 Purity ≥ 98.5%, maximum single unknown impurity ≤ 0.2%, total impurities ≤ 1.5% |
90357-53-2 N-[4-CYANO-3-(TRIFLUOROMETHYL)PHENYL]-2-METHACRYLAMIDE.pdf
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N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methacrylamide is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .
China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.
yes , you can have 1 N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methacrylamide sample for starting the business , but it is not free
please contact sale team for detail .
This compound's structure makes it suitable for several applications:
Polymerization: The methacrylate group can undergo radical polymerization, making it a useful building block for creating polymers or copolymers with specific properties, such as high stability, resistance to degradation, or enhanced electronic properties.
Organic Synthesis: The cyano group and trifluoromethyl group can make this molecule a valuable intermediate for synthesizing more complex organic compounds, especially those that require electron-withdrawing groups for enhanced reactivity or stability.
Medicinal Chemistry: The cyano and trifluoromethyl groups are often found in bioactive molecules. This compound could be explored for its potential as a lead compound in drug discovery, particularly for targeting receptors or enzymes with a high affinity for compounds with such functional groups.
Material Science: Due to its methacrylamide backbone, the compound could be incorporated into polymeric materials, such as adhesives, coatings, and films. Its combination of electron-withdrawing groups might also make it useful in organic electronics or sensor devices.
The cyano group (-C≡N) is an electron-withdrawing group that increases the polarity of the molecule and enhances its reactivity. The cyano group can participate in various chemical reactions, including:
Nucleophilic addition reactions, where the cyano group can serve as an electrophilic site for nucleophilic attack.
Stabilization of reactive intermediates, as the electron-withdrawing nature of the cyano group can help stabilize transition states in certain chemical reactions.
Additionally, the cyano group can increase the compound's solubility in polar solvents and influence its bioactivity in medicinal applications.
Toxicity: Like many organic compounds with reactive groups (such as the cyano group), this compound may be toxic if ingested, inhaled, or absorbed through the skin. Always use appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat.
Reactivity: The presence of the methacrylate and cyano groups means the compound can undergo reactions under certain conditions. Handle with care, especially when using solvents or initiating polymerization reactions.
Flammability: The compound may be flammable, particularly in its pure form. Avoid heat, sparks, and open flames when handling the substance.
Dispose of the compound in accordance with local hazardous waste disposal regulations.
Due to the presence of potentially toxic or reactive groups, the compound should be handled by a certified waste disposal service.
If dealing with significant quantities, consult with a professional disposal service to ensure proper neutralization or treatment of the compound before disposal.