(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid

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Reagent Code: #36264
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CAS Number 161601-29-2

science Other reagents with same CAS 161601-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD02259726
thermostat Physical Properties
Boiling Point 382.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly in the synthesis of peptides and peptidomimetics. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino functionality during multi-step synthetic processes, allowing for selective deprotection and further functionalization. This compound is often employed in the development of drug candidates, especially those targeting enzymes or receptors where cyclopentane-based structures are advantageous. Its stereochemistry also makes it valuable in creating chiral molecules, which are essential for producing enantiomerically pure pharmaceuticals. Additionally, it finds utility in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of therapeutic agents.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,276.00
inventory 100mg
10-20 days ฿8,199.00

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(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid
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(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly in the synthesis of peptides and peptidomimetics. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino functionality during multi-step synthetic processes, allowing for selective deprotection and further func

(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly in the synthesis of peptides and peptidomimetics. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino functionality during multi-step synthetic processes, allowing for selective deprotection and further functionalization. This compound is often employed in the development of drug candidates, especially those targeting enzymes or receptors where cyclopentane-based structures are advantageous. Its stereochemistry also makes it valuable in creating chiral molecules, which are essential for producing enantiomerically pure pharmaceuticals. Additionally, it finds utility in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of therapeutic agents.

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