Fmoc-L-Indoline-2-carboxylic acid

98%

Reagent Code: #105091
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CAS Number 198560-38-2

science Other reagents with same CAS 198560-38-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.41 g/mol
Formula C₂₄H₁₉NO₄
badge Registry Numbers
MDL Number MFCD00273469
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Fmoc-L-Indoline-2-carboxylic acid is widely used in peptide synthesis as a building block. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the stepwise assembly of peptides. The compound is employed to introduce the indoline moiety into peptide chains, which can enhance the biological activity or stability of the resulting peptides. It is also utilized in the development of peptidomimetics and bioactive molecules, where the indoline structure plays a critical role in mimicking natural peptide conformations or interacting with biological targets. Additionally, it finds application in medicinal chemistry research for designing and synthesizing novel drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,382.00

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Fmoc-L-Indoline-2-carboxylic acid
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Fmoc-L-Indoline-2-carboxylic acid is widely used in peptide synthesis as a building block. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the stepwise assembly of peptides. The compound is employed to introduce the indoline moiety into peptide chains, which can enhance the biological activity or stability of the resulting peptides. It is also utilized in the development of peptidomimetics and bioactive molecules, where the indol
Fmoc-L-Indoline-2-carboxylic acid is widely used in peptide synthesis as a building block. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the stepwise assembly of peptides. The compound is employed to introduce the indoline moiety into peptide chains, which can enhance the biological activity or stability of the resulting peptides. It is also utilized in the development of peptidomimetics and bioactive molecules, where the indoline structure plays a critical role in mimicking natural peptide conformations or interacting with biological targets. Additionally, it finds application in medicinal chemistry research for designing and synthesizing novel drug candidates.
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