(1R,2R)-2-((tert-Butoxycarbonyl)amino)cyclohexanecarboxylic acid

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Reagent Code: #231165
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CAS Number 233661-54-6

science Other reagents with same CAS 233661-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.30 g/mol
Formula C₁₂H₂₁NO₄
badge Registry Numbers
MDL Number MFCD04974225
thermostat Physical Properties
Boiling Point 396.7±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Widely used in organic synthesis, particularly in the pharmaceutical industry, as a chiral building block for the preparation of bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds, especially in the development of peptidomimetics and protease inhibitors. Commonly employed in multi-step syntheses where preservation of stereochemical integrity is critical. The Boc-protected amine and carboxylic acid functionalities allow for selective deprotection and coupling reactions, making it ideal for solid-phase and solution-phase peptide synthesis. Also utilized in the design of conformationally constrained intermediates for drug discovery programs targeting central nervous system disorders and metabolic diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,880.00
inventory 250mg
10-20 days ฿9,360.00
inventory 1g
10-20 days ฿24,420.00
inventory 5g
10-20 days ฿99,720.00
(1R,2R)-2-((tert-Butoxycarbonyl)amino)cyclohexanecarboxylic acid
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Widely used in organic synthesis, particularly in the pharmaceutical industry, as a chiral building block for the preparation of bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds, especially in the development of peptidomimetics and protease inhibitors. Commonly employed in multi-step syntheses where preservation of stereochemical integrity is critical. The Boc-protected amine and carboxylic acid functionalities allow for selective deprotection an

Widely used in organic synthesis, particularly in the pharmaceutical industry, as a chiral building block for the preparation of bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds, especially in the development of peptidomimetics and protease inhibitors. Commonly employed in multi-step syntheses where preservation of stereochemical integrity is critical. The Boc-protected amine and carboxylic acid functionalities allow for selective deprotection and coupling reactions, making it ideal for solid-phase and solution-phase peptide synthesis. Also utilized in the design of conformationally constrained intermediates for drug discovery programs targeting central nervous system disorders and metabolic diseases.

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