N-α-Benzoyl-L-histidine
CAS: 5354-94-9
Ref. 3D-FB47552
5g | To inquire | ||
10g | To inquire | ||
25g | To inquire | ||
50g | To inquire |
Product Information
- Bz-L-His-OH
- (2S)-2-Benzamido-3-(1H-imidazol-3-ium-5-yl)propanoate
- (2S)-3-(1H-Imidazol-4-yl)-2-(phenylformamido)propanoic acid
- (S)-2-Benzoylamino-3-(1H-imidazol-4-yl)propanoic acid
- <span class="text-smallcaps">L</span>-Histidine, N-benzoyl-
- Histidine, N-benzoyl-, <span class="text-smallcaps">L</span>-
- N-Alpha-Benzoyl-L-Histidine
- N-Benzoyl-<span class="text-smallcaps">L</span>-histidine
- N-Benzoylhistidine
- N<sup>α</sup>-Benzoyl-<span class="text-smallcaps">L</span>-histidine
- See more synonyms
- N<sup>α</sup>-Benzoylhistidine
- NSC 306118
- α-N-Benzoyl-<span class="text-smallcaps">L</span>-histidine
- L-Histidine, N-benzoyl-
- N-Benzoyl-L-histidine
- Histidine, N-benzoyl-, L-
- α-N-Benzoyl-L-histidine
Benzoyl-L-histidine is a derivative of the amino acid histidine, which is a regulatory molecule in biochemical reactions. It has been shown to be an isomeric form of benzoyl-L-histidine. Benzoyl-L-histidine has been shown to be oxidized by bromoacetic acid and titrated with potassium permanganate. This reaction produces a residue, which can be quantified by the use of a thiolate reagent and model system. Benzoyl-L-histidine has two isomers: monosubstituted and disubstituted. The kinetic properties of this compound have also been studied in a model protein system.
Chemical properties
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