N-Ethyl-4-(trifluoromethyl)benzylamine
≥95%
- Product Code: 69618
CAS:
90390-12-8
Molecular Weight: | 203.20 g./mol | Molecular Formula: | C₁₀H₁₂F₃N |
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EC Number: | MDL Number: | MFCD09948554 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Ethyl-4-(trifluoromethyl)benzylamine is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the preparation of more complex chemical compounds. Its structure, featuring an ethyl group and a trifluoromethylbenzyl moiety, makes it particularly valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is crucial in drug design. Additionally, this compound is often employed in the synthesis of biologically active molecules, including potential therapeutic agents targeting neurological disorders and other diseases. Its reactivity and functional groups allow for further derivatization, enabling the creation of diverse chemical libraries for screening and optimization purposes.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to brown liquid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿4,450.00 |
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5.000 | 10-20 days | ฿11,800.00 |
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N-Ethyl-4-(trifluoromethyl)benzylamine
N-Ethyl-4-(trifluoromethyl)benzylamine is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the preparation of more complex chemical compounds. Its structure, featuring an ethyl group and a trifluoromethylbenzyl moiety, makes it particularly valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is crucial in drug design. Additionally, this compound is often employed in the synthesis of biologically active molecules, including potential therapeutic agents targeting neurological disorders and other diseases. Its reactivity and functional groups allow for further derivatization, enabling the creation of diverse chemical libraries for screening and optimization purposes.
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