(1R,2R)-2-[(tert-Butoxycarbonylamino)methyl]cyclopropanecarboxylic acid

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Reagent Code: #228721
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CAS Number 952708-48-4

science Other reagents with same CAS 952708-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.2463 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD28501612
thermostat Physical Properties
Boiling Point 367.3±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.186±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antidiabetic agents. Its cyclopropane scaffold with defined stereochemistry enables precise control over molecular conformation in active pharmaceutical ingredients. Commonly employed in peptide mimetics and protease inhibitor designs due to its ability to stabilize specific backbone geometries. The Boc-protected amine and carboxylic acid functionalities allow for straightforward coupling and deprotection steps in multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,920.00
inventory 1g
10-20 days ฿33,130.00
(1R,2R)-2-[(tert-Butoxycarbonylamino)methyl]cyclopropanecarboxylic acid
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Used as a key chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antidiabetic agents. Its cyclopropane scaffold with defined stereochemistry enables precise control over molecular conformation in active pharmaceutical ingredients. Commonly employed in peptide mimetics and protease inhibitor designs due to its ability to stabilize specific backbone geometries. The Boc-protected amine and carboxylic acid functionalities allow for straigh

Used as a key chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antidiabetic agents. Its cyclopropane scaffold with defined stereochemistry enables precise control over molecular conformation in active pharmaceutical ingredients. Commonly employed in peptide mimetics and protease inhibitor designs due to its ability to stabilize specific backbone geometries. The Boc-protected amine and carboxylic acid functionalities allow for straightforward coupling and deprotection steps in multi-step organic syntheses.

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