Phenyl (R)-(1-cyclohexylethyl)carbamate

98%

Reagent Code: #229556
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CAS Number 1786598-19-3

science Other reagents with same CAS 1786598-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.33 g/mol
Formula C₁₅H₂₁NO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the separation of chiral amines and alcohols. Its asymmetric structure enables selective interaction with enantiomeric compounds, making it valuable in analytical chemistry and pharmaceutical synthesis for obtaining optically pure intermediates. Commonly applied in HPLC and capillary electrophoresis to improve enantiomeric separation. Also serves as a building block in the synthesis of chiral catalysts and auxiliaries for asymmetric reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿7,130.00
5g
10-20 days ฿24,940.00
Phenyl (R)-(1-cyclohexylethyl)carbamate
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Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the separation of chiral amines and alcohols. Its asymmetric structure enables selective interaction with enantiomeric compounds, making it valuable in analytical chemistry and pharmaceutical synthesis for obtaining optically pure intermediates. Commonly applied in HPLC and capillary electrophoresis to improve enantiomeric separation. Also serves as a building block in the synthesis of chiral catalysts and auxiliaries f

Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the separation of chiral amines and alcohols. Its asymmetric structure enables selective interaction with enantiomeric compounds, making it valuable in analytical chemistry and pharmaceutical synthesis for obtaining optically pure intermediates. Commonly applied in HPLC and capillary electrophoresis to improve enantiomeric separation. Also serves as a building block in the synthesis of chiral catalysts and auxiliaries for asymmetric reactions.

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