rel-(1R-2E-pR)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate

≥96%, rel-(1R-2E-pR)-equatorial

Reagent Code: #229192
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CAS Number 2645443-14-5

science Other reagents with same CAS 2645443-14-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.3 g/mol
Formula C₁₅H₁₇NO₅
thermostat Physical Properties
Boiling Point 433.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its cyclic carbonate structure enables selective reactions with nucleophiles, making it valuable in the development of pharmaceutical intermediates where stereochemical control is critical. Commonly employed in catalytic asymmetric transformations, such as ring-opening reactions, to generate functionalized building blocks with high enantioselectivity. Also utilized in the study of chiral recognition and in the design of chiral catalysts or ligands for enantioselective catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿20,100.00
100mg
10-20 days ฿65,020.00
250mg
10-20 days ฿130,030.00
rel-(1R-2E-pR)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate
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Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its cyclic carbonate structure enables selective reactions with nucleophiles, making it valuable in the development of pharmaceutical intermediates where stereochemical control is critical. Commonly employed in catalytic asymmetric transformations, such as ring-opening reactions, to generate functionalized building blocks with high enantioselectivity. Also utilized in the study of
Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its cyclic carbonate structure enables selective reactions with nucleophiles, making it valuable in the development of pharmaceutical intermediates where stereochemical control is critical. Commonly employed in catalytic asymmetric transformations, such as ring-opening reactions, to generate functionalized building blocks with high enantioselectivity. Also utilized in the study of chiral recognition and in the design of chiral catalysts or ligands for enantioselective catalysis.
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