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Home  > (S)-2-((tert-Butoxycarbonyl)amino)-3-(1-methyl-1h-indol-3-yl)propanoic acid

AW00390

109927-44-8 | (S)-2-((tert-Butoxycarbonyl)amino)-3-(1-methyl-1h-indol-3-yl)propanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $13.00 $10.00 -   +
250mg 98% in stock $29.00 $21.00 -   +
1g 98% in stock $116.00 $82.00 -   +
10g 98% in stock $915.00 $641.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AW00390
Chemical Name: (S)-2-((tert-Butoxycarbonyl)amino)-3-(1-methyl-1h-indol-3-yl)propanoic acid
CAS Number: 109927-44-8
Molecular Formula: C17H22N2O4
Molecular Weight: 318.3676
MDL Number: MFCD28987645
SMILES: O=C(OC(C)(C)C)N[C@H](C(=O)O)Cc1cn(c2c1cccc2)C

 

Upstream Synthesis Route
  • The (S)-2-((tert-Butoxycarbonyl)amino)-3-(1-methyl-1H-indol-3-yl)propanoic acid is a valuable compound used in chemical synthesis for peptide and drug development. Its unique structure allows for precise control over the stereochemistry of amino acid incorporation in peptide synthesis. With its tert-butoxycarbonyl (Boc) protecting group, this compound serves as a crucial building block in the construction of complex peptide sequences. By selectively deprotecting and activating the amino group, chemists can efficiently introduce this amino acid derivative into peptide chains, enabling the creation of tailor-made peptides with desired functionalities. In the field of drug discovery, this compound plays a vital role in the synthesis of peptide-based drug candidates that target specific biological pathways. Its versatility and compatibility with standard peptide synthesis methodologies make it a versatile tool for organic chemists working in the pharmaceutical and biotechnology industries.
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