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Home  > Methyl 2-amino-3-(1h-indol-3-yl)-2-methylpropanoate

AA18771

114524-80-0 | Methyl 2-amino-3-(1h-indol-3-yl)-2-methylpropanoate

Packsize Purity Availability Price Discounted Price    Quantity
25mg 97% in stock $141.00 $99.00 -   +
50mg 97% in stock $163.00 $114.00 -   +
100mg 97% in stock $259.00 $182.00 -   +
250mg 97% in stock $493.00 $345.00 -   +
1g 97% in stock $969.00 $678.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA18771
Chemical Name: Methyl 2-amino-3-(1h-indol-3-yl)-2-methylpropanoate
CAS Number: 114524-80-0
Molecular Formula: C13H16N2O2
Molecular Weight: 232.2783
MDL Number: MFCD00152138
SMILES: COC(=O)C(Cc1c[nH]c2c1cccc2)(N)C

 

Upstream Synthesis Route
  • As a professional chemist, I can attest to the versatile applications of Tryptophan, Nα-methyl-, methyl ester in chemical synthesis. This compound serves as a valuable building block in organic chemistry, particularly in the creation of complex molecules and pharmaceuticals. Its unique structure and properties make it a crucial component in the development of novel compounds.Tryptophan, Nα-methyl-, methyl ester is frequently utilized in the synthesis of peptides and proteins due to its ability to introduce specific functional groups and tailor molecular structures. Its role in peptide synthesis is particularly notable, as it can be incorporated into peptide chains to modulate their properties and functions. Additionally, this compound is instrumental in the preparation of various drug candidates and bioactive compounds, where its presence can influence the pharmacological characteristics of the final product.Moreover, Tryptophan, Nα-methyl-, methyl ester is an essential tool in chemical research and development, enabling chemists to explore new synthetic pathways and strategies. Its use in asymmetric synthesis and chiral transformations has significant implications for the production of enantiopure compounds with enhanced biological activity and selectivity. By leveraging the reactivity and selectivity of this compound, researchers can access a wide range of structurally diverse molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.
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