(R)-1-(9H-Fluoren-9-yl)ethanol

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Reagent Code: #113457
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CAS Number 107474-78-2

science Other reagents with same CAS 107474-78-2

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Weight 210.27 g/mol
Formula C₁₅H₁₄O
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

(R)-1-(9H-Fluoren-9-yl)ethanol is primarily utilized in the field of organic synthesis, particularly in the development of chiral compounds. Its structure, featuring a fluorenyl group, makes it a valuable intermediate in asymmetric synthesis, where it aids in the creation of enantiomerically pure substances. This is crucial in pharmaceutical research, as the chirality of a molecule can significantly impact its biological activity. Additionally, it is employed in the preparation of complex organic molecules, serving as a building block in the synthesis of ligands, catalysts, and other fine chemicals. Its role in facilitating stereoselective reactions underscores its importance in advancing synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,462.00
inventory 100mg
10-20 days ฿3,870.00
inventory 1g
10-20 days ฿17,442.00

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(R)-1-(9H-Fluoren-9-yl)ethanol
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(R)-1-(9H-Fluoren-9-yl)ethanol is primarily utilized in the field of organic synthesis, particularly in the development of chiral compounds. Its structure, featuring a fluorenyl group, makes it a valuable intermediate in asymmetric synthesis, where it aids in the creation of enantiomerically pure substances. This is crucial in pharmaceutical research, as the chirality of a molecule can significantly impact its biological activity. Additionally, it is employed in the preparation of complex organic molecul

(R)-1-(9H-Fluoren-9-yl)ethanol is primarily utilized in the field of organic synthesis, particularly in the development of chiral compounds. Its structure, featuring a fluorenyl group, makes it a valuable intermediate in asymmetric synthesis, where it aids in the creation of enantiomerically pure substances. This is crucial in pharmaceutical research, as the chirality of a molecule can significantly impact its biological activity. Additionally, it is employed in the preparation of complex organic molecules, serving as a building block in the synthesis of ligands, catalysts, and other fine chemicals. Its role in facilitating stereoselective reactions underscores its importance in advancing synthetic methodologies.

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