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Structure of 19652-32-5
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N-Fmoc-L-alanine is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Alanine is one of the simplest amino acids - a methyl group as the side chain. This small side chain confers a high degree of flexibility when incorporated into a polypeptide chain. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.
3-Bromo-5-chloro-2-hydroxybenzaldehyde serves as a versatile building block for the synthesis of substituted benzene derivatives and heterocyclic scaffolds. Its strategic placement of bromo, chloro, and hydroxy groups enables selective functionalization via cross-coupling, electrophilic substitution, or protection strategies. The aldehyde functionality facilitates condensation reactions, while the phenolic hydroxyl group offers opportunities for derivatization or metal coordination. Bench-stable and compatible with standard purification methods, it supports efficient workflow integration in medicinal chemistry and materials science applications.
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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: