CAS 30033-24-0
:N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine
Description:
N-(tert-Butoxycarbonyl)-3,4-dihydroxy-L-phenylalanine, commonly referred to as Boc-DOPA, is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino group of L-DOPA. This compound features a phenylalanine backbone with two hydroxyl groups located at the 3 and 4 positions of the aromatic ring, contributing to its unique reactivity and solubility properties. Boc-DOPA is typically used in peptide synthesis and as an intermediate in the production of various pharmaceuticals, particularly those targeting neurological conditions due to its structural similarity to neurotransmitters. The Boc group serves to protect the amino functionality during synthetic processes, allowing for selective reactions at other functional sites. In terms of physical properties, Boc-DOPA is generally a white to off-white solid, soluble in polar solvents, and stable under standard laboratory conditions. Its reactivity can be influenced by the presence of the hydroxyl groups, which can participate in hydrogen bonding and other interactions, making it a versatile compound in organic synthesis and medicinal chemistry.
Formula:C14H19NO6
Synonyms:- N-(tert-Butyloxycarbonyl)-L-dopa
- N-(tert-Buloxycarbonyl)-3-hydroxy-L-tyrosine
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Found 4 products.
N-(tert-buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine
CAS:Formula:C14H19NO6Purity:95%Color and Shape:SolidMolecular weight:297.3038(S)-2-((tert-Butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoic acid
CAS:<p>(S)-2-((tert-Butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoic acid</p>Purity:95%Molecular weight:297.30g/mol(S)-2-((tert-Butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoic acid
CAS:Purity:95%Molecular weight:297.3070068N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine
CAS:<p>N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine is a biomimetic that is used for the immobilization of enzymes. It has been shown to have high resistance to enzymatic and chemical degradation. The immobilized enzyme can be used in the treatment of intestinal diseases caused by bacteria or salinity. N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine has also been used as a coating material to protect metal surfaces from corrosion and oxidation. This compound is synthesized using trifluoroacetic acid and hydrogen gas with a primary amine catalyst. Coordination chemistry is involved in the synthesis of this compound.</p>Formula:C14H19NO6Purity:Min. 95%Molecular weight:297.3 g/mol



