1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid

95%

  • Product Code: 39589
  CAS:    208772-41-2
Molecular Weight: 263.2891 g./mol Molecular Formula: C₁₄H₁₇NO₄
EC Number: MDL Number: MFCD09878909
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in organic synthesis as a building block for more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. Its tert-butoxycarbonyl (Boc) protecting group is crucial for shielding the amine functionality during multi-step synthetic processes, allowing selective reactions to occur without interference. The carboxylic acid group provides a reactive site for further modifications, such as amide bond formation, which is essential in drug development. Its application is particularly relevant in the synthesis of indoline-based compounds, which are often explored for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities.
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Size (g) Availability Price Quantity
0.100 10-20 days ฿5,985.00
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1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid
This chemical is primarily used in organic synthesis as a building block for more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, including potential drug candidates. Its tert-butoxycarbonyl (Boc) protecting group is crucial for shielding the amine functionality during multi-step synthetic processes, allowing selective reactions to occur without interference. The carboxylic acid group provides a reactive site for further modifications, such as amide bond formation, which is essential in drug development. Its application is particularly relevant in the synthesis of indoline-based compounds, which are often explored for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities.
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