cis-1-(tert-butoxycarbonyl)pyrrolidine-3,4-dicarboxylic acid

95%

Reagent Code: #55702
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CAS Number 1782350-51-9

science Other reagents with same CAS 1782350-51-9

blur_circular Chemical Specifications

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Weight 259.26 g/mol
Formula C₁₁H₁₇NO₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and dicarboxylic acid functionality, makes it valuable for selective reactions and peptide synthesis. The Boc group can be easily removed under mild conditions, allowing for further modifications. Additionally, its pyrrolidine ring is often incorporated into compounds targeting neurological disorders, inflammation, and other therapeutic areas. This compound is also used in the study of enzyme inhibitors and receptor modulators due to its ability to mimic natural substrates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,700.00
inventory 5g
10-20 days ฿53,820.00

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cis-1-(tert-butoxycarbonyl)pyrrolidine-3,4-dicarboxylic acid
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This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and dicarboxylic acid functionality, makes it valuable for selective reactions and peptide synthesis. The Boc group can be easily removed under mild conditions, allowing for further modifications. A

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and dicarboxylic acid functionality, makes it valuable for selective reactions and peptide synthesis. The Boc group can be easily removed under mild conditions, allowing for further modifications. Additionally, its pyrrolidine ring is often incorporated into compounds targeting neurological disorders, inflammation, and other therapeutic areas. This compound is also used in the study of enzyme inhibitors and receptor modulators due to its ability to mimic natural substrates.

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