Product Information
- Z-L-alanyl-L-phenylalanineN-Carbobenzoxy-L-alanyl-L-phenylalanine
- <span class="text-smallcaps">L</smallcap>-Phenylalanine, N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-alanyl-
- <span class="text-smallcaps">L</smallcap>-Phenylalanine, N-[N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-alanyl]-
- Alanine, N-(N-carboxy-<span class="text-smallcaps">L</smallcap>-alanyl)-3-phenyl-, N-benzyl ester, <smallcap>L</span>-
- Alanine, N-(N-carboxyalanyl)-3-phenyl-, N-benzyl ester
- Carbobenzoxy-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-phenylalanine
- N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-phenylalanine
- N-Carbobenzyloxy-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-phenylalanine
- N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-phenylalanine
- N-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanine
- See more synonyms
- N-[(benzyloxy)carbonyl]alanylphenylalanine
- NSC 87854
Z-Ala-Phe-OH is an amino acid with the chemical formula CH3CH(NH2)CO2H. It is a white, water-soluble solid that is used in immobilization chemistry and surface methodology to increase the efficiency of catalysis. Z-Ala-Phe-OH is also an intermediate in the synthesis of caffeine, a stimulant found in coffee beans. The biological function of this amino acid has not been determined, but it has been shown to be a substrate for serine proteases and amide hydrolysis. The catalysed reaction between Z-Ala-Phe-OH and phosgene produces carbonyl groups.
Chemical properties
Technical inquiry about: 3D-FA48879 Z-Ala-Phe-OH
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