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*For research and further manufacturing use only, not for direct human use.
Structure of 162545-29-1
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This fluorenylmethoxycarbonyl-protected amino acid derivative integrates seamlessly into peptide synthesis workflows. The 9H-fluoren-9-ylmethoxy carbonyl group enables efficient, orthogonal protection of amine functionalities, offering high stability under standard reaction conditions and clean deprotection with mild acids.
2-{Ethyl[(9H-fluoren-9-ylmethoxy)carbonyl]amino}acetic acid serves as a versatile protected amino acid building block, enabling efficient peptide synthesis via solid-phase and solution-phase methods. The Fmoc group provides excellent stability under basic conditions and facilitates orthogonal deprotection, while the ethyl ester allows for selective hydrolysis or further functionalization. Its bench-stable, crystalline nature supports straightforward handling and purification, making it ideal for iterative coupling protocols in medicinal chemistry and API development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: