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AA33013

119768-45-5 | Boc-5-hydroxy-l-tryptophan

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $147.00 $103.00 -   +
5g 97% in stock $310.00 $217.00 -   +
25g 97% in stock $798.00 $559.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA33013
Chemical Name: Boc-5-hydroxy-l-tryptophan
CAS Number: 119768-45-5
Molecular Formula: C16H20N2O5
Molecular Weight: 320.3404
MDL Number: MFCD00270732
SMILES: OC(=O)[C@H](Cc1c[nH]c2c1cc(O)cc2)NC(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • The compound (S)-2-((tert-Butoxycarbonyl)amino)-3-(5-hydroxy-1H-indol-3-yl)propanoic acid, commonly referred to as $name$, serves as a valuable building block in chemical synthesis. This compound is frequently utilized as a key intermediate in the preparation of various pharmaceuticals and organic compounds.In chemical synthesis, (S)-2-((tert-Butoxycarbonyl)amino)-3-(5-hydroxy-1H-indol-3-yl)propanoic acid plays a crucial role in the creation of complex molecules due to its unique structural features. Its incorporation enables the introduction of both the amino and hydroxy functionalities into the desired organic molecules with high efficiency.Moreover, the presence of the tert-butoxycarbonyl (Boc) protecting group in this compound provides control over the reactivity of the amino group, allowing for selective transformations during the synthesis process. This versatile building block exhibits excellent compatibility with a variety of chemical reactions, facilitating the formation of intricate molecular structures with precision.Overall, the application of (S)-2-((tert-Butoxycarbonyl)amino)-3-(5-hydroxy-1H-indol-3-yl)propanoic acid in chemical synthesis serves as a fundamental strategy for constructing diverse molecules in the field of medicinal chemistry and organic synthesis.
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