(+)-1-(9-Fluorenyl)ethyl chloroformate is an organic compound characterized by its chloroformate functional group, which is known for its reactivity in various chemical transformations. This substance features a fluorenyl moiety, contributing to its unique structural and electronic properties. The presence of the chloroformate group makes it a useful reagent in organic synthesis, particularly in the formation of esters and in the protection of alcohols. The compound is typically a colorless to pale yellow liquid, and it is sensitive to moisture, which can lead to hydrolysis. It is important to handle this compound with care due to its potential reactivity and the presence of chlorine, which can pose health hazards. As with many chloroformates, it may release toxic gases upon decomposition or reaction with water. Its applications are primarily found in synthetic organic chemistry, where it serves as an intermediate in the preparation of more complex molecules. Proper safety measures and protocols should be followed when working with this substance in a laboratory setting.

(+)-1-(9-FLUORENYL)ETHYL CHLOROFORMATE

105764-39-4: (-)-Flec Solution,50 Mg In 10 Ml Acetone, (+)-Flec(Tm), (-)-Flec(R), (-)-Flec, (-)-1-(9-Fluorenyl)ethylchloroformate, 1-(9H-fluoren-9-yl)ethyl carbonochloridate, (1S)-1-(9H-fluoren-9-yl)ethyl chlorocarbonate, (1R)-1-(9H-fluoren-9-yl)ethyl chlorocarbonate,  (-)-1-(9-FLUORENYL)ETHYL CHLOROFORMATE

CAS 105764-39-4: (+)-1-(9-FLUORENYL)ETHYL CHLOROFORMATE

1-(9H-Fluoren-9-yl)ethyl carbonochloridate

Ref: 4Z-A-233006