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Structure of 1171331-39-7
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2-Amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride delivers a trifluoromethylated amine scaffold with enhanced solubility and metabolic stability. The electron-withdrawing trifluoromethyl group modulates basicity while maintaining compatibility with standard peptide coupling protocols. This bench-stable salt form facilitates direct incorporation into bioactive molecule synthesis.
2-Amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated amide-containing scaffolds. The trifluoroethyl group imparts enhanced metabolic stability and lipophilicity, while the aminoacetamide functionality facilitates downstream coupling reactions. Its crystalline hydrochloride salt form ensures excellent bench stability, ease of handling, and straightforward purification—key attributes for scalable API development and high-throughput screening workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: