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

≥96%

Reagent Code: #229200
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CAS Number 2645443-13-4

science Other reagents with same CAS 2645443-13-4

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 enriched compounds. Its cyclic carbonate structure enables selective ring-opening reactions, making it valuable in the development of chiral building blocks for pharmaceuticals and fine chemicals. Commonly employed in catalytic kinetic resolution and desymmetrization processes due to its well-defined stereochemistry and reactivity toward nucleophiles. Also serves as an intermediate in the synthesis of complex natural products where stereocontrol is critical.

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inventory 100mg
10-20 days ฿74,590.00

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rel-(1R-2E-pS)-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 enriched compounds. Its cyclic carbonate structure enables selective ring-opening reactions, making it valuable in the development of chiral building blocks for pharmaceuticals and fine chemicals. Commonly employed in catalytic kinetic resolution and desymmetrization processes due to its well-defined stereochemistry and reactivity toward nucleophiles. Also serves as an intermediate in the synt

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the preparation of enantiomerically enriched compounds. Its cyclic carbonate structure enables selective ring-opening reactions, making it valuable in the development of chiral building blocks for pharmaceuticals and fine chemicals. Commonly employed in catalytic kinetic resolution and desymmetrization processes due to its well-defined stereochemistry and reactivity toward nucleophiles. Also serves as an intermediate in the synthesis of complex natural products where stereocontrol is critical.

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