(S)-1-(tert-Butoxycarbonyl)indoline-2-carboxylic acid

95%

Reagent Code: #236487
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CAS Number 144069-67-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
badge Registry Numbers
MDL Number MFCD00273433
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug intermediates. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in asymmetric synthesis due to its stereochemical purity, it serves as a key intermediate in the preparation of indoline-based compounds with potential neurological and cardiovascular activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies and in the construction of complex natural product analogs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿830.00
inventory 1g
10-20 days ฿2,410.00
inventory 5g
10-20 days ฿6,440.00
inventory 25g
10-20 days ฿22,830.00
(S)-1-(tert-Butoxycarbonyl)indoline-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug intermediates. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in asymmetric synthesis due to its stereochemical purity, it serves as a key intermediate in the preparation of indoline-based compounds with potential neurological and cardiovascular activity. Also utilized in medicinal chem

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug intermediates. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in asymmetric synthesis due to its stereochemical purity, it serves as a key intermediate in the preparation of indoline-based compounds with potential neurological and cardiovascular activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies and in the construction of complex natural product analogs.

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