N-Benzyl-2,2,2-trifluoroacetamide
≥95%
- Product Code: 121552
CAS:
7387-69-1
| Molecular Weight: | 203.16 g./mol | Molecular Formula: | C₉H₈F₃NO |
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| EC Number: | MDL Number: | MFCD00188542 | |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Benzyl-2,2,2-trifluoroacetamide is primarily utilized in organic synthesis as a versatile intermediate. It is commonly employed in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic properties. The trifluoroacetamide group in the molecule is often used to enhance the stability and reactivity of the compounds during chemical reactions. Additionally, it serves as a protecting group for amines in peptide synthesis, ensuring selective reactions without unwanted side interactions. Its application extends to the field of agrochemicals, where it is used in the synthesis of active ingredients for crop protection products. The compound's unique structure also makes it valuable in research for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | €64.35 |
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| 1.000 | 10-20 days | €217.73 |
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N-Benzyl-2,2,2-trifluoroacetamide
N-Benzyl-2,2,2-trifluoroacetamide is primarily utilized in organic synthesis as a versatile intermediate. It is commonly employed in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic properties. The trifluoroacetamide group in the molecule is often used to enhance the stability and reactivity of the compounds during chemical reactions. Additionally, it serves as a protecting group for amines in peptide synthesis, ensuring selective reactions without unwanted side interactions. Its application extends to the field of agrochemicals, where it is used in the synthesis of active ingredients for crop protection products. The compound's unique structure also makes it valuable in research for studying reaction mechanisms and developing new synthetic methodologies.
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