Ethyl (1R,2R)-2-ethylcyclopropane-1-carboxylate

97%

Reagent Code: #229332
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CAS Number 1932008-66-6

science Other reagents with same CAS 1932008-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.2 g/mol
Formula C₈H₁₄O₂
thermostat Physical Properties
Boiling Point 171.2±8.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.981±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of chiral pharmaceutical intermediates, particularly in the development of active ingredients requiring high enantiomeric purity. Its strained cyclopropane ring and ester functionality make it valuable in ring-opening reactions and carbon-chain elongation processes. Commonly employed in asymmetric synthesis to introduce stereodefined ethyl-substituted cyclopropane motifs found in bioactive molecules. Also utilized in agrochemical research for building structurally rigid frameworks that enhance metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,670.00
inventory 250mg
10-20 days ฿26,610.00
inventory 1g
10-20 days ฿71,600.00
Ethyl (1R,2R)-2-ethylcyclopropane-1-carboxylate
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Used in the synthesis of chiral pharmaceutical intermediates, particularly in the development of active ingredients requiring high enantiomeric purity. Its strained cyclopropane ring and ester functionality make it valuable in ring-opening reactions and carbon-chain elongation processes. Commonly employed in asymmetric synthesis to introduce stereodefined ethyl-substituted cyclopropane motifs found in bioactive molecules. Also utilized in agrochemical research for building structurally rigid frameworks t

Used in the synthesis of chiral pharmaceutical intermediates, particularly in the development of active ingredients requiring high enantiomeric purity. Its strained cyclopropane ring and ester functionality make it valuable in ring-opening reactions and carbon-chain elongation processes. Commonly employed in asymmetric synthesis to introduce stereodefined ethyl-substituted cyclopropane motifs found in bioactive molecules. Also utilized in agrochemical research for building structurally rigid frameworks that enhance metabolic stability.

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